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Publication DateJournal of craniofacial genetics and developmental biology, ISSN 0270-4145, 1981
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The Cleft palate-craniofacial journal, ISSN 1055-6656, 1991
Journal
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2008, 2nd ed., ISBN 9781860949937, xii, 492
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Molecular Cytogenetics, ISSN 1755-8166, 10/2016, Volume 9, Issue 1, pp. 1 - 5
Background: Interstitial microdeletions in 1p are extremely rare, as very few cases have been reported postnatally and only one prenatally, yet. There is a...
Genotype-phenotype correlation | Prenatal diagnosis | Chromosome 1 | Microdeletions | Array-based Comparative Genomic Hybridization array (a-CGH) | PROTEIN | GENETICS & HEREDITY | SNIP1 | BINDING | FAMILY | Facial asymmetry | Gene mutations | Physiological aspects | Genetic aspects | Diagnosis | Research
Genotype-phenotype correlation | Prenatal diagnosis | Chromosome 1 | Microdeletions | Array-based Comparative Genomic Hybridization array (a-CGH) | PROTEIN | GENETICS & HEREDITY | SNIP1 | BINDING | FAMILY | Facial asymmetry | Gene mutations | Physiological aspects | Genetic aspects | Diagnosis | Research
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Loading RightsCell, ISSN 0092-8674, 06/2006, Volume 125, Issue 5, pp. 971 - 986
Vertebrate skeletogenesis involves two processes, skeletal patterning and osteoblast differentiation. Here, we show that , encoding a nuclear matrix protein,...
CLEFT-PALATE | ELEMENTS | MAR-BINDING PROTEIN | OSTEOCALCIN GENE | HOMEOTIC TRANSFORMATION | CRANIAL NEURAL CREST | BONE-FORMATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | MATRIX ATTACHMENT REGIONS | GENE-EXPRESSION | CELL BIOLOGY | Facial Bones - abnormalities | Gene Expression Regulation, Developmental - genetics | Craniofacial Abnormalities - physiopathology | Genes, Homeobox - genetics | Cell Differentiation - genetics | Branchial Region - abnormalities | Branchial Region - cytology | Skull - abnormalities | Osteoblasts - cytology | Craniofacial Abnormalities - metabolism | Craniofacial Abnormalities - genetics | Osteogenesis - genetics | Facial Bones - metabolism | Branchial Region - metabolism | Activating Transcription Factor 4 - genetics | Repressor Proteins - genetics | Transcription Factors - genetics | Mutation - genetics | Homeodomain Proteins - genetics | Mice, Knockout | Animals | Matrix Attachment Region Binding Proteins - genetics | Mice | Osteoblasts - metabolism | Body Patterning - genetics | Core Binding Factor Alpha 1 Subunit - genetics | Genetic research | Genetic code | Genetic aspects | Research | Craniofacial abnormalities | Translocation (Genetics) | Analysis | DNA binding proteins
CLEFT-PALATE | ELEMENTS | MAR-BINDING PROTEIN | OSTEOCALCIN GENE | HOMEOTIC TRANSFORMATION | CRANIAL NEURAL CREST | BONE-FORMATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | MATRIX ATTACHMENT REGIONS | GENE-EXPRESSION | CELL BIOLOGY | Facial Bones - abnormalities | Gene Expression Regulation, Developmental - genetics | Craniofacial Abnormalities - physiopathology | Genes, Homeobox - genetics | Cell Differentiation - genetics | Branchial Region - abnormalities | Branchial Region - cytology | Skull - abnormalities | Osteoblasts - cytology | Craniofacial Abnormalities - metabolism | Craniofacial Abnormalities - genetics | Osteogenesis - genetics | Facial Bones - metabolism | Branchial Region - metabolism | Activating Transcription Factor 4 - genetics | Repressor Proteins - genetics | Transcription Factors - genetics | Mutation - genetics | Homeodomain Proteins - genetics | Mice, Knockout | Animals | Matrix Attachment Region Binding Proteins - genetics | Mice | Osteoblasts - metabolism | Body Patterning - genetics | Core Binding Factor Alpha 1 Subunit - genetics | Genetic research | Genetic code | Genetic aspects | Research | Craniofacial abnormalities | Translocation (Genetics) | Analysis | DNA binding proteins
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Loading RightsJournal of Pediatrics, The, ISSN 0022-3476, 2014, Volume 164, Issue 3, pp. 458 - 462.e2
Objective To review the clinical characteristics in a series of 25 patients with VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with...
Pediatrics | MALFORMATIONS | THUMB | DYSPLASIA | PEDIATRICS | TETHERED SPINAL-CORD | CONGENITAL-ANOMALIES | VATER ASSOCIATION | DEFICIENCY | Facial Bones - abnormalities | Urogenital Abnormalities - epidemiology | Umbilical Arteries - abnormalities | Humans | Limb Deformities, Congenital - therapy | Male | Odontoid Process - abnormalities | Spine - abnormalities | Orthopedic Procedures | Female | Trachea - abnormalities | Neural Tube Defects - epidemiology | Sacrococcygeal Region - abnormalities | Linear Models | Radius - abnormalities | Esophagus - abnormalities | Anal Canal - abnormalities | Limb Deformities, Congenital - diagnosis | Kidney - abnormalities | Limb Deformities, Congenital - epidemiology | Coccyx - abnormalities | Heart Defects, Congenital - epidemiology | Heart Defects, Congenital - diagnosis | Heart Defects, Congenital - therapy | Thumb - abnormalities | Fistula, Tracheoesophageal | Medical genetics
Pediatrics | MALFORMATIONS | THUMB | DYSPLASIA | PEDIATRICS | TETHERED SPINAL-CORD | CONGENITAL-ANOMALIES | VATER ASSOCIATION | DEFICIENCY | Facial Bones - abnormalities | Urogenital Abnormalities - epidemiology | Umbilical Arteries - abnormalities | Humans | Limb Deformities, Congenital - therapy | Male | Odontoid Process - abnormalities | Spine - abnormalities | Orthopedic Procedures | Female | Trachea - abnormalities | Neural Tube Defects - epidemiology | Sacrococcygeal Region - abnormalities | Linear Models | Radius - abnormalities | Esophagus - abnormalities | Anal Canal - abnormalities | Limb Deformities, Congenital - diagnosis | Kidney - abnormalities | Limb Deformities, Congenital - epidemiology | Coccyx - abnormalities | Heart Defects, Congenital - epidemiology | Heart Defects, Congenital - diagnosis | Heart Defects, Congenital - therapy | Thumb - abnormalities | Fistula, Tracheoesophageal | Medical genetics
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Loading RightsThe Journal of craniofacial surgery, ISSN 1049-2275, 09/2018, Volume 29, Issue 6, pp. 1633 - 1637
Although facial paralysis is a fundamental feature of hemifacial microsomia, the frequency and distribution of nerve abnormalities in patients with hemifacial...
microtia | OMENS classification system | SURGERY | hemifacial microsomia | ANOMALIES | Facial paralysis | PLUS CLASSIFICATION | PALSY | CRANIOFACIAL MICROSOMIA | FEATURES | Facial Bones - abnormalities | Congenital Microtia - complications | Humans | Congenital Microtia - surgery | Male | Facial Asymmetry - epidemiology | Facial Nerve - abnormalities | Goldenhar Syndrome - surgery | Goldenhar Syndrome - diagnosis | Facial Bones - surgery | Adult | Congenital Microtia - epidemiology | Female | Facial Bones - diagnostic imaging | Facial Paralysis - epidemiology | Goldenhar Syndrome - complications | Severity of Illness Index | Goldenhar Syndrome - epidemiology | Risk Assessment | Ear - abnormalities | Congenital Microtia - diagnosis | Facial Asymmetry - etiology | Facial Paralysis - diagnosis | Facial Asymmetry - diagnosis | Facial Paralysis - etiology | Facial Bones - innervation | Facial asymmetry | Complications and side effects | Development and progression | Care and treatment | Paralysis, Facial
microtia | OMENS classification system | SURGERY | hemifacial microsomia | ANOMALIES | Facial paralysis | PLUS CLASSIFICATION | PALSY | CRANIOFACIAL MICROSOMIA | FEATURES | Facial Bones - abnormalities | Congenital Microtia - complications | Humans | Congenital Microtia - surgery | Male | Facial Asymmetry - epidemiology | Facial Nerve - abnormalities | Goldenhar Syndrome - surgery | Goldenhar Syndrome - diagnosis | Facial Bones - surgery | Adult | Congenital Microtia - epidemiology | Female | Facial Bones - diagnostic imaging | Facial Paralysis - epidemiology | Goldenhar Syndrome - complications | Severity of Illness Index | Goldenhar Syndrome - epidemiology | Risk Assessment | Ear - abnormalities | Congenital Microtia - diagnosis | Facial Asymmetry - etiology | Facial Paralysis - diagnosis | Facial Asymmetry - diagnosis | Facial Paralysis - etiology | Facial Bones - innervation | Facial asymmetry | Complications and side effects | Development and progression | Care and treatment | Paralysis, Facial
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Loading Rights1994, ISBN 0723610177, 178
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Developmental Dynamics, ISSN 1058-8388, 02/2011, Volume 240, Issue 2, pp. 365 - 371
We have previously demonstrated that Gpr177, the mouse orthologue of Drosophila Wls/Evi/Srt, is required for establishment of the anterior–posterior axis. The...
Wnt production | Wnt signaling | β‐catenin | neural crest | Sprinter | Evi | Gpr177 | Wntless | β-catenin | Neural crest | beta-catenin | MOUSE EMBRYOGENESIS | ANATOMY & MORPHOLOGY | DEVELOPMENTAL BIOLOGY | INT-1 PROTOONCOGENE | DELETION | MUTANT MICE | SIGNALING PATHWAY | AXIS FORMATION | EXPRESSION | MIDBRAIN | Facial Bones - abnormalities | Wnt1 Protein - genetics | Brain - embryology | Receptors, G-Protein-Coupled - metabolism | Craniofacial Abnormalities - embryology | Mice, Transgenic | Intracellular Signaling Peptides and Proteins - metabolism | Wnt1 Protein - metabolism | Brain - abnormalities | Facial Bones - embryology | Wnt Proteins - metabolism | Gene Knockdown Techniques | Skull - embryology | Animals | Wnt Proteins - genetics | Skull - abnormalities | Craniofacial Abnormalities - pathology | Wnt3 Protein | Mice | Receptors, G-Protein-Coupled - genetics | Wnt3A Protein | Intracellular Signaling Peptides and Proteins - genetics | Craniofacial Abnormalities - genetics
Wnt production | Wnt signaling | β‐catenin | neural crest | Sprinter | Evi | Gpr177 | Wntless | β-catenin | Neural crest | beta-catenin | MOUSE EMBRYOGENESIS | ANATOMY & MORPHOLOGY | DEVELOPMENTAL BIOLOGY | INT-1 PROTOONCOGENE | DELETION | MUTANT MICE | SIGNALING PATHWAY | AXIS FORMATION | EXPRESSION | MIDBRAIN | Facial Bones - abnormalities | Wnt1 Protein - genetics | Brain - embryology | Receptors, G-Protein-Coupled - metabolism | Craniofacial Abnormalities - embryology | Mice, Transgenic | Intracellular Signaling Peptides and Proteins - metabolism | Wnt1 Protein - metabolism | Brain - abnormalities | Facial Bones - embryology | Wnt Proteins - metabolism | Gene Knockdown Techniques | Skull - embryology | Animals | Wnt Proteins - genetics | Skull - abnormalities | Craniofacial Abnormalities - pathology | Wnt3 Protein | Mice | Receptors, G-Protein-Coupled - genetics | Wnt3A Protein | Intracellular Signaling Peptides and Proteins - genetics | Craniofacial Abnormalities - genetics
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Loading RightsJournal of Dental Research, ISSN 0022-0345, 3/2016, Volume 95, Issue 3, pp. 302 - 310
The craniofacial skeleton is derived from both neural crest cells and mesodermal cells; however, the majority of the bone, cartilage, and connective tissue is...
dentin sialophosphoprotein | mandible | odontoblasts | calvaria | dental pulp | mineralization | BIOMINERALIZATION | ODONTOBLAST DIFFERENTIATION | TEETH | MATRIX PROTEINS | SIALOPHOSPHOPROTEIN DSPP | GENE | SIALOPROTEIN | DENTISTRY, ORAL SURGERY & MEDICINE | BONE | EXPRESSION | Facial Bones - abnormalities | Sialoglycoproteins - genetics | Nerve Tissue Proteins - analysis | Alveolar Process - abnormalities | Core Binding Factor Alpha 1 Subunit - analysis | Integrin-Binding Sialoprotein - analysis | Membrane Proteins - analysis | Sialoglycoproteins - physiology | Kruppel-Like Transcription Factors - analysis | Cranial Sutures - abnormalities | Skull - abnormalities | Dentinogenesis - physiology | Phosphates - blood | Facial Bones - growth & development | Matrix Metalloproteinase 2 - analysis | Phosphoproteins - physiology | Organ Culture Techniques | Dentin - abnormalities | Fibronectins - analysis | Extracellular Matrix Proteins - genetics | Calcification, Physiologic - physiology | Extracellular Matrix Proteins - physiology | Matrix Metalloproteinase 9 - analysis | Phosphoproteins - genetics | Mutation - genetics | Osteoblasts - pathology | Receptors, Notch - analysis | Animals | Collagen Type I - analysis | Mice | Odontogenesis - physiology | Zinc Finger Protein GLI1 | Osteopontin - analysis | Skull - growth & development | Research Reports
dentin sialophosphoprotein | mandible | odontoblasts | calvaria | dental pulp | mineralization | BIOMINERALIZATION | ODONTOBLAST DIFFERENTIATION | TEETH | MATRIX PROTEINS | SIALOPHOSPHOPROTEIN DSPP | GENE | SIALOPROTEIN | DENTISTRY, ORAL SURGERY & MEDICINE | BONE | EXPRESSION | Facial Bones - abnormalities | Sialoglycoproteins - genetics | Nerve Tissue Proteins - analysis | Alveolar Process - abnormalities | Core Binding Factor Alpha 1 Subunit - analysis | Integrin-Binding Sialoprotein - analysis | Membrane Proteins - analysis | Sialoglycoproteins - physiology | Kruppel-Like Transcription Factors - analysis | Cranial Sutures - abnormalities | Skull - abnormalities | Dentinogenesis - physiology | Phosphates - blood | Facial Bones - growth & development | Matrix Metalloproteinase 2 - analysis | Phosphoproteins - physiology | Organ Culture Techniques | Dentin - abnormalities | Fibronectins - analysis | Extracellular Matrix Proteins - genetics | Calcification, Physiologic - physiology | Extracellular Matrix Proteins - physiology | Matrix Metalloproteinase 9 - analysis | Phosphoproteins - genetics | Mutation - genetics | Osteoblasts - pathology | Receptors, Notch - analysis | Animals | Collagen Type I - analysis | Mice | Odontogenesis - physiology | Zinc Finger Protein GLI1 | Osteopontin - analysis | Skull - growth & development | Research Reports
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Loading RightsDevelopmental Biology, ISSN 0012-1606, 07/2014, Volume 391, Issue 2, pp. 170 - 181
Congenital bony syngnathia, a rare but severe human birth defect, is characterized by bony fusion of the mandible to the maxilla. However, the genetic...
Cleft palate | Syngnathia | Cranial neural crest | Bmp signaling | Craniofacial patterning | CLEFT-PALATE | SIGNALING PATHWAYS | SECONDARY PALATE | MOUSE | DEVELOPMENTAL BIOLOGY | INDUCTION | TOOTH | MICE EXHIBIT | MORPHOGENESIS | CRANIOFACIAL DEVELOPMENT | MSX1 | Facial Bones - abnormalities | Mandible - abnormalities | Wnt1 Protein - genetics | Neural Crest - cytology | Maxilla - embryology | Bone Morphogenetic Protein 4 - genetics | Humans | Mice, Inbred C57BL | Bone Morphogenetic Protein Receptors, Type I - genetics | Cleft Palate - embryology | Mice, Transgenic | Cleft Palate - genetics | Signal Transduction - genetics | Facial Bones - embryology | Bone Morphogenetic Protein Receptors, Type I - biosynthesis | Bone Morphogenetic Protein 4 - biosynthesis | Neural Crest - metabolism | Mandible - embryology | Animals | Maxilla - abnormalities | Facial Bones - growth & development | Mice | Models, Genetic | Jaw Abnormalities - genetics | Bone morphogenetic proteins | Fibroblast growth factors | Genetic engineering | Birth defects | Gene expression | Analysis | cleft palate | craniofacial patterning | cranial neural crest | syngnathia
Cleft palate | Syngnathia | Cranial neural crest | Bmp signaling | Craniofacial patterning | CLEFT-PALATE | SIGNALING PATHWAYS | SECONDARY PALATE | MOUSE | DEVELOPMENTAL BIOLOGY | INDUCTION | TOOTH | MICE EXHIBIT | MORPHOGENESIS | CRANIOFACIAL DEVELOPMENT | MSX1 | Facial Bones - abnormalities | Mandible - abnormalities | Wnt1 Protein - genetics | Neural Crest - cytology | Maxilla - embryology | Bone Morphogenetic Protein 4 - genetics | Humans | Mice, Inbred C57BL | Bone Morphogenetic Protein Receptors, Type I - genetics | Cleft Palate - embryology | Mice, Transgenic | Cleft Palate - genetics | Signal Transduction - genetics | Facial Bones - embryology | Bone Morphogenetic Protein Receptors, Type I - biosynthesis | Bone Morphogenetic Protein 4 - biosynthesis | Neural Crest - metabolism | Mandible - embryology | Animals | Maxilla - abnormalities | Facial Bones - growth & development | Mice | Models, Genetic | Jaw Abnormalities - genetics | Bone morphogenetic proteins | Fibroblast growth factors | Genetic engineering | Birth defects | Gene expression | Analysis | cleft palate | craniofacial patterning | cranial neural crest | syngnathia
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Loading RightsPLoS ONE, ISSN 1932-6203, 09/2011, Volume 6, Issue 9, p. e24608
The planar cell polarity effector gene Fuz regulates ciliogenesis and Fuz loss of function studies reveal an array of embryonic phenotypes. However, cilia...
PRIMARY CILIA FORMATION | GENE | AUTOSOMAL SEX REVERSAL | CRANIAL NEURAL CREST | CAMPOMELIC DYSPLASIA | MULTIDISCIPLINARY SCIENCES | PLANAR CELL POLARITY | CONVERGENT EXTENSION | MECKELS CARTILAGE | SONIC-HEDGEHOG | NEGATIVE REGULATOR | Facial Bones - abnormalities | Humans | Craniofacial Abnormalities - embryology | Male | Intracellular Signaling Peptides and Proteins - metabolism | Hedgehog Proteins | In Situ Hybridization | Chromatin Immunoprecipitation | Gene Expression Regulation, Developmental | Mice, Mutant Strains | Polymerase Chain Reaction | Skull - abnormalities | Female | Craniofacial Abnormalities - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Wnt Signaling Pathway | CHO Cells | Cell Line | Cricetinae | Facial Bones - metabolism | Skull - metabolism | beta Catenin | Mice, Inbred C57BL | Signal Transduction - genetics | Facial Bones - embryology | Skull - embryology | Animals | Fluorescent Antibody Technique | Signal Transduction - physiology | Mice | Embryonic development | Chromatin | Cell proliferation | Pediatrics | Tongue | Transcription factors | Deformation | Wnt protein | Mesenchyme | Genomics | Genes | Feedback loops | Defects | Ossification | Proteins | Cartilage | β-catenin | Signal transduction | Embryogenesis | Negative feedback | Pathways | Animal tissues | Incisors | Polarity | Localization | Cilia | Mandible | Gene expression | Cleft lip/palate | Embryonic growth stage | Studies | Craniofacial growth | Signaling | Insects | Hedgehog protein | MicroRNAs | Control theory | Anophthalmia | Binding sites
PRIMARY CILIA FORMATION | GENE | AUTOSOMAL SEX REVERSAL | CRANIAL NEURAL CREST | CAMPOMELIC DYSPLASIA | MULTIDISCIPLINARY SCIENCES | PLANAR CELL POLARITY | CONVERGENT EXTENSION | MECKELS CARTILAGE | SONIC-HEDGEHOG | NEGATIVE REGULATOR | Facial Bones - abnormalities | Humans | Craniofacial Abnormalities - embryology | Male | Intracellular Signaling Peptides and Proteins - metabolism | Hedgehog Proteins | In Situ Hybridization | Chromatin Immunoprecipitation | Gene Expression Regulation, Developmental | Mice, Mutant Strains | Polymerase Chain Reaction | Skull - abnormalities | Female | Craniofacial Abnormalities - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Wnt Signaling Pathway | CHO Cells | Cell Line | Cricetinae | Facial Bones - metabolism | Skull - metabolism | beta Catenin | Mice, Inbred C57BL | Signal Transduction - genetics | Facial Bones - embryology | Skull - embryology | Animals | Fluorescent Antibody Technique | Signal Transduction - physiology | Mice | Embryonic development | Chromatin | Cell proliferation | Pediatrics | Tongue | Transcription factors | Deformation | Wnt protein | Mesenchyme | Genomics | Genes | Feedback loops | Defects | Ossification | Proteins | Cartilage | β-catenin | Signal transduction | Embryogenesis | Negative feedback | Pathways | Animal tissues | Incisors | Polarity | Localization | Cilia | Mandible | Gene expression | Cleft lip/palate | Embryonic growth stage | Studies | Craniofacial growth | Signaling | Insects | Hedgehog protein | MicroRNAs | Control theory | Anophthalmia | Binding sites
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In vivo impact of Dlx3 conditional inactivation in neural crest‐derived craniofacial bones
Journal of Cellular Physiology, ISSN 0021-9541, 03/2013, Volume 228, Issue 3, pp. 654 - 664
Mutations in DLX3 in humans lead to defects in craniofacial and appendicular bones, yet the in vivo activities related to Dlx3 function during normal skeletal...
TARGETED DISRUPTION | PHYSIOLOGY | MURINE DENTITION | HOMEODOMAIN PROTEINS | CALCITONIN-GENE | MICE | DIFFERENTIATION | SKELETAL | EXPRESSION | TDO SYNDROME | HOMEOBOX GENES | CELL BIOLOGY | Facial Bones - abnormalities | Mandible - abnormalities | Osteogenesis - physiology | Transcription Factors - physiology | Bone Density - physiology | Humans | Transcription Factors - deficiency | Male | Bone Density - genetics | Transcription Factors - genetics | Homeodomain Proteins - genetics | Mice, Knockout | Pregnancy | Animals | Gene Expression Regulation, Developmental | Base Sequence | Skull - abnormalities | Female | Mice | Homeodomain Proteins - physiology | Neural Crest - abnormalities | Osteogenesis - genetics | Bones | Density | Genes | Analysis | Craniofacial | Dlx3 | Neural crest | development bone
TARGETED DISRUPTION | PHYSIOLOGY | MURINE DENTITION | HOMEODOMAIN PROTEINS | CALCITONIN-GENE | MICE | DIFFERENTIATION | SKELETAL | EXPRESSION | TDO SYNDROME | HOMEOBOX GENES | CELL BIOLOGY | Facial Bones - abnormalities | Mandible - abnormalities | Osteogenesis - physiology | Transcription Factors - physiology | Bone Density - physiology | Humans | Transcription Factors - deficiency | Male | Bone Density - genetics | Transcription Factors - genetics | Homeodomain Proteins - genetics | Mice, Knockout | Pregnancy | Animals | Gene Expression Regulation, Developmental | Base Sequence | Skull - abnormalities | Female | Mice | Homeodomain Proteins - physiology | Neural Crest - abnormalities | Osteogenesis - genetics | Bones | Density | Genes | Analysis | Craniofacial | Dlx3 | Neural crest | development bone
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Loading RightsJournal of Oral and Maxillofacial Surgery, ISSN 0278-2391, 2014, Volume 72, Issue 6, pp. 1173 - 1179
Purpose Premature closure of the spheno-occipital synchondrosis (SOS) has been associated with midface hypoplasia in animal models and patients with specific...
Surgery | FUSION | CRANIAL BASE | DENTISTRY, ORAL SURGERY & MEDICINE | FACIAL GROWTH | MUTATION | APERTS SYNDROME | CLOSURE | SKULL | OSTEOGENESIS | BONE | CRANIOSYNOSTOSIS | Facial Bones - abnormalities | Sphenoid Bone - abnormalities | Age Factors | Sphenoid Bone - growth & development | Humans | Child, Preschool | Tomography, X-Ray Computed - methods | Infant | Male | Case-Control Studies | Young Adult | Cranial Sutures - abnormalities | Craniofacial Dysostosis - physiopathology | Cranial Sutures - diagnostic imaging | Facial Bones - growth & development | Female | Facial Bones - diagnostic imaging | Child | Occipital Bone - abnormalities | Calcification, Physiologic - physiology | Craniofacial Dysostosis - diagnostic imaging | Sphenoid Bone - diagnostic imaging | Occipital Bone - diagnostic imaging | Cranial Sutures - growth & development | Adolescent | Occipital Bone - growth & development | Radiology | Sects | Surgery, Plastic | Radiology, Medical | College teachers | Comparative analysis
Surgery | FUSION | CRANIAL BASE | DENTISTRY, ORAL SURGERY & MEDICINE | FACIAL GROWTH | MUTATION | APERTS SYNDROME | CLOSURE | SKULL | OSTEOGENESIS | BONE | CRANIOSYNOSTOSIS | Facial Bones - abnormalities | Sphenoid Bone - abnormalities | Age Factors | Sphenoid Bone - growth & development | Humans | Child, Preschool | Tomography, X-Ray Computed - methods | Infant | Male | Case-Control Studies | Young Adult | Cranial Sutures - abnormalities | Craniofacial Dysostosis - physiopathology | Cranial Sutures - diagnostic imaging | Facial Bones - growth & development | Female | Facial Bones - diagnostic imaging | Child | Occipital Bone - abnormalities | Calcification, Physiologic - physiology | Craniofacial Dysostosis - diagnostic imaging | Sphenoid Bone - diagnostic imaging | Occipital Bone - diagnostic imaging | Cranial Sutures - growth & development | Adolescent | Occipital Bone - growth & development | Radiology | Sects | Surgery, Plastic | Radiology, Medical | College teachers | Comparative analysis
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Loading RightsL' Orthodontie francaise, ISSN 0078-6608, 12/2016, Volume 87, Issue 4, p. 479
Since the beginning of cephalometric analysis, a significant number of approaches to vertical facial proportions have been proposed. In our view, diagnosing a...
Facial Bones - abnormalities | Abnormalities, Multiple - therapy | Face - abnormalities | Humans | Syndrome
Facial Bones - abnormalities | Abnormalities, Multiple - therapy | Face - abnormalities | Humans | Syndrome
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