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1. Journal of craniofacial genetics and developmental biology
Society of Craniofacial Genetics
Journal of craniofacial genetics and developmental biology, ISSN 0270-4145, 1981
Skull | Periodicals | Developmental biology | Growth | Abnormalities
Journal
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2. Malformations
by Vinken, P. J and Myrianthopoulos, Ntinos C
1987, ISBN 9780444904614, Volume 50., xv, 669
Brain | Skull | Spine | Abnormalities | Central nervous system
Book
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3. Craniofacial embryogenetics and development
by Sperber, Geoffrey H and Guttmann, Geoffrey D and Sperber, Steven M
2010, 2nd ed., ISBN 9781607950325, 250
Head | growth & development | Maxillofacial Development | Maxillofacial Abnormalities | Growth | abnormalities | Teeth | Facial Bones | Developmental genetics | genetics | Embryology, Human | Skull | Craniofacial Abnormalities
Book
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4. Orthodontics & craniofacial research
Orthodontics & craniofacial research, ISSN 1601-6335, 2002
Orthodontics | Orthodontics, Corrective | Orthodontic appliances
Journal
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5. Full Text Dental and Cranial Pathologies in Mice Lacking the Cl−/H+‐Exchanger ClC‐7
by Wen, Xin and Lacruz, Rodrigo S and Paine, Michael L
The Anatomical Record, ISSN 1932-8486, 08/2015, Volume 298, Issue 8, pp. 1502 - 1508
ABSTRACT ClC‐7 is a 2Cl−/1H+‐exchanger expressed at late endosomes and lysosomes, as well as the ruffled border of osteoclasts. ClC‐7 deficiencies in mice and... 
craniofacial development | biomineralization | chloride channels | enamel | ameloblast | pH regulation | amelogenesis | Craniofacial development | Amelogenesis | Enamel | Biomineralization | Chloride channels | Ameloblast | PH regulation | ENAMEL MATURATION | PHYSIOLOGY | ANATOMY & MORPHOLOGY | REQUIRES OSTM1 | GENETICS | TRANSPORT ACTIVITY | DISEASE | AMELOBLASTS | OSTEOPETROSIS | INSIGHTS | Tooth - ultrastructure | Tooth Abnormalities - metabolism | Chloride Channels - deficiency | Chloride Channels - genetics | X-Ray Microtomography | Ameloblasts - pathology | Craniofacial Abnormalities - diagnostic imaging | Ameloblasts - metabolism | Dentinogenesis | Cranial Sutures - abnormalities | Skull - abnormalities | Craniofacial Abnormalities - pathology | Craniofacial Abnormalities - metabolism | Craniofacial Abnormalities - genetics | Microscopy, Electron, Scanning | Tooth Abnormalities - genetics | Ameloblasts - ultrastructure | Dentin - abnormalities | Genotype | Bone Development | Mice, Knockout | Phenotype | Animals | Skull - diagnostic imaging | Dental Enamel - abnormalities | Tooth Abnormalities - pathology | Tooth - metabolism | Tooth - pathology
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6. Full Text Anterior skull base duplication requiring delivery via EXIT procedure: A case report
by Shires, Courtney B and Giurintano, Jonathan P and McLevy-Bazzanella, Jennifer and Thompson, Jerome
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 12/2018, Volume 115, pp. 24 - 26
Duplication of the anterior skull base structures is an extremely rare malformation of failed midline blastogenesis. We present the case of a child with an... 
Procedure | Airway | EXIT | PEDIATRICS | OTORHINOLARYNGOLOGY | Cerebral Aqueduct - abnormalities | Pituitary Gland - abnormalities | Humans | Skull Base - diagnostic imaging | Basilar Artery - abnormalities | Abnormalities, Multiple - diagnostic imaging | Craniofacial Abnormalities - surgery | Tracheotomy | Abnormalities, Multiple - surgery | Craniofacial Abnormalities - diagnostic imaging | Delivery, Obstetric - methods | Maxilla - abnormalities | Skull Base - abnormalities | Ultrasonography, Prenatal | Female | Child
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7. Craniofacial development
by Chai, Yang, editor
2015, Current topics in developmental biology, ISBN 9780124081413, Volume 115, xxiii, 644 pages
Craniofacial Development, the latest volume of Current Topics in Developmental Biology continues the legacy of this premier serial with quality chapters... 
Facial bones | Head | growth & development | Maxillofacial Development | Growth | Skull | Craniofacial Abnormalities | Molecular aspects | Developmental biology | Face | Embryology, Human
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8. Full Text Evolution of the radiographic appearance of the metaphyses over the first year of life in type V osteogenesis imperfecta: Clues to pathogenesis
by Arundel, Paul and Offiah, Amaka and Bishop, Nicholas J
Journal of Bone and Mineral Research, ISSN 0884-0431, 04/2011, Volume 26, Issue 4, pp. 894 - 898
We present the first report of the development of characteristic radiologic appearances of long bones during the first year of life in an infant with type V... 
RICKETS | PEDIATRICS | OSTEOGENESIS IMPERFECTA | GROWTH PLATE | RADIOLOGY | Osteogenesis imperfecta | growth plate | rickets | radiology | pediatrics | MUTATION | DISEASE | ENDOCRINOLOGY & METABOLISM | CHONDRODYSPLASIA | Growth Plate - pathology | Fetus - abnormalities | Leg Bones - pathology | Humans | Fetus - pathology | Ulna - abnormalities | Bone Diseases, Metabolic - pathology | Leg Bones - diagnostic imaging | Tibia - pathology | Growth Plate - abnormalities | Ribs - abnormalities | Ribs - diagnostic imaging | Ulna - pathology | Ulna - diagnostic imaging | Skull - pathology | Skull - abnormalities | Diphosphonates - therapeutic use | Cranial Fontanelles - abnormalities | Osteogenesis Imperfecta - etiology | Infant, Newborn | Arm Bones - diagnostic imaging | Plagiocephaly - pathology | Arm Bones - pathology | Osteogenesis Imperfecta - drug therapy | Tibia - diagnostic imaging | Bone Density Conservation Agents - therapeutic use | Osteogenesis Imperfecta - diagnostic imaging | Fibula - abnormalities | Radiography | Skull - diagnostic imaging | Growth Plate - diagnostic imaging | Femoral Fractures - pathology | Spine - abnormalities | Tibia - abnormalities | Rib Fractures - diagnostic imaging | Female | Ribs - pathology | Fractures, Bone - diagnostic imaging | Spine - pathology | Rib Fractures - pathology | Fibula - pathology | Cranial Fontanelles - pathology | Bone Diseases, Metabolic - diagnostic imaging | Pamidronate | Spine - diagnostic imaging | Ultrasonography, Prenatal | Leg Bones - abnormalities | Osteogenesis Imperfecta - pathology | Fractures, Bone - pathology | Vitamin D - therapeutic use | Longitudinal Studies | Arm Bones - abnormalities
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9. Full Text Flat feline faces: Is brachycephaly associated with respiratory abnormalities in the domestic cat (Felis catus)?
by Farnworth, Mark J and Chen, Ruoning and Packer, Rowena M. A and Caney, Sarah M. A and Gunn-Moore, Danièlle A
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, p. e0161777
There has been little research into brachycephalism and associated disorders in cats. A questionnaire aimed at cat owners was used to determine the... 
DISORDERS | AIRWAY SYNDROME | BREED | MULTIDISCIPLINARY SCIENCES | DOGS | Cats | Life Style | Lung Diseases - veterinary | Lung Diseases - diagnosis | Craniosynostoses - complications | Humans | Cat Diseases - diagnosis | Linear Models | Male | Craniosynostoses - veterinary | Animals | Bonding, Human-Pet | Skull - abnormalities | Female | Care and treatment | Research | Diagnosis | Risk factors | Diseases | Animal models | Breeding | Abnormalities | Staining | Risk analysis | Breeding of animals | Physical properties | Tearing | Grooming | Nose | Physical characteristics | Mouth | Questionnaires | Dogs | Position measurement | Skull | Photographs | Breathing | Conformation
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10. Full Text Craniocervical junction abnormalities in dogs
by Dewey, C W and Marino, D J and Loughin, C A
New Zealand Veterinary Journal, ISSN 0048-0169, 07/2013, Volume 61, Issue 4, pp. 202 - 211
Craniocervical junction abnormality (CJA) is a term that encompasses a number of developmental anatomical aberrations at the region of the caudal occiput and... 
Chiari-like malformation | atlanto-occipital overlap | syringomyelia | Craniocervical junction abnormality | atlantoaxial instability | BASILAR INVAGINATION | TREATED PATIENTS | CEREBROSPINAL-FLUID | OCCIPITAL BONE HYPOPLASIA | I MALFORMATION | ATLANTOAXIAL SUBLUXATION | CRANIOVERTEBRAL REALIGNMENT | KING-CHARLES SPANIELS | VETERINARY SCIENCES | SMALL-BREED DOGS | Atlanto-occipital joint | Syringomyelia | Dogs | Cervical Vertebrae - abnormalities | Dog Diseases - congenital | Trauma, Nervous System - veterinary | Animals | Skull - abnormalities
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11. Full Text p38 inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice
by Wang, Yingli and Zhou, Xueyan and Oberoi, Kurun and Phelps, Robert and Couwenhoven, Ross and Sun, Miao and Rezza, Amélie and Holmes, Greg and Percival, Christopher J and Friedenthal, Jenna and Krejci, Pavel and Richtsmeier, Joan T and Huso, David L and Rendl, Michael and Jabs, Ethylin Wang
Journal of Clinical Investigation, ISSN 0021-9738, 06/2012, Volume 122, Issue 6, pp. 2153 - 2164
Beare-Stevenson cutis gyrata syndrome (BSS) is a human genetic disorder characterized by skin and skull abnormalities. BSS is caused by mutations in the FGF... 
MEDICINE, RESEARCH & EXPERIMENTAL | ACTIVATED PROTEIN-KINASE | OSTEOBLAST DIFFERENTIATION | ACANTHOSIS NIGRICANS | APERT-SYNDROME | CUTIS-GYRATA-SYNDROME | SKELETAL DYSPLASIA | GROWTH-FACTOR RECEPTOR-2 | DEVELOPMENTAL DELAY | CROUZON-SYNDROME | LYS650MET MUTATION | Abnormalities, Multiple - pathology | Receptor, Fibroblast Growth Factor, Type 2 - metabolism | Humans | Craniosynostoses - enzymology | Abnormalities, Multiple - drug therapy | Mutation, Missense | Acanthosis Nigricans - genetics | Craniosynostoses - drug therapy | Skull - abnormalities | Skin Abnormalities - drug therapy | p38 Mitogen-Activated Protein Kinases - metabolism | Acanthosis Nigricans - enzymology | Skin Abnormalities - pathology | Abnormalities, Multiple - genetics | Skin Abnormalities - enzymology | Acanthosis Nigricans - drug therapy | Craniosynostoses - genetics | p38 Mitogen-Activated Protein Kinases - genetics | Mice, Transgenic | Syndrome | Acanthosis Nigricans - pathology | Animals | MAP Kinase Signaling System - drug effects | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | Abnormalities, Multiple - enzymology | Skin Abnormalities - genetics | Mice | Protein Kinase Inhibitors - pharmacology | Craniosynostoses - pathology | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Amino Acid Substitution | Care and treatment | Beare-Stevenson cutis gyrata syndrome | Diagnosis
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12. Full Text SATB2 Is a Multifunctional Determinant of Craniofacial Patterning and Osteoblast Differentiation
by Dobreva, Gergana and Chahrour, Maria and Dautzenberg, Marcel and Chirivella, Laura and Kanzler, Benoit and Fariñas, Isabel and Karsenty, Gerard and Grosschedl, Rudolf
Cell, 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
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13. Full Text P53 coordinates cranial neural crest cell growth and epithelial-mesenchymal transition/delamination processes
by Rinon, Ariel and Molchadsky, Alina and Nathan, Elisha and Yovel, Gili and Rotter, Varda and Sarig, Rachel and Tzahor, Eldad
Development, ISSN 0950-1991, 05/2011, Volume 138, Issue 9, pp. 1827 - 1838
Neural crest development involves epithelial-mesenchymal transition (EMT), during which epithelial cells are converted into individual migratory cells.... 
Craniofacial development | Epithelial-mesenchymal transition | Mouse | Cranial neural crest | Chick | EMT | P53 | PROGENITOR CELLS | CARDIAC OUTFLOW TRACT | TUBE DEFECTS | MUSCLE | DEVELOPMENTAL BIOLOGY | SLUG | p53 | P53-MEDIATED APOPTOSIS | MESODERM | DIFFERENTIATION | EXPRESSION | EMBRYOS | Cell Proliferation | Embryo, Mammalian | Epithelial-Mesenchymal Transition - physiology | Craniofacial Abnormalities - embryology | Musculoskeletal Abnormalities - complications | Epithelial-Mesenchymal Transition - genetics | Musculoskeletal Abnormalities - pathology | Musculoskeletal Abnormalities - embryology | Tumor Suppressor Protein p53 - genetics | Neural Crest - metabolism | Tumor Suppressor Protein p53 - physiology | Craniofacial Abnormalities - pathology | Craniofacial Abnormalities - complications | Craniofacial Abnormalities - genetics | Neural Crest - cytology | Skull - metabolism | Mice, Inbred C57BL | Cells, Cultured | Tumor Suppressor Protein p53 - metabolism | Mice, Transgenic | Chick Embryo | Skull - embryology | Animals | Neural Crest - embryology | Musculoskeletal Abnormalities - genetics | Mice | Laminin - metabolism
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14. Full Text Understanding craniofacial anomalies
: the etiopathogenesis of craniosynostoses and facial clefting
by Mooney, Mark P and Siegel, Michael I
2002, ISBN 047138724X
Skull | Cleft palate | Craniosynostoses | Genetic aspects | Face | Abnormalities
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15. The Cleft palate-craniofacial journal
: official publication of the American Cleft Palate-Craniofacial Association
and American Cleft Palate-Craniofacial AssociationAmerican Cleft Palate Association
The Cleft palate-craniofacial journal, ISSN 1055-6656, 1991
Periodicals | Skull | Cleft palate | Face | Abnormalities | Surgery
Journal
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16. Full Text Re: Risk of ultrasound‐detected neonatal brain abnormalities in intrauterine growth‐restricted fetuses born between 28 and 34 weeks' gestation: relationship with gestational age at birth and fetal Doppler parameters. R. Cruz‐Martinez, V. Tenorio, N. Padilla, F. Crispi, F. Figueras and E. Gratacós. Ultrasound Obstet Gynecol 2015; 46: 452–459
by Morales‐Roselló, J
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 10/2015, Volume 46, Issue 4, pp. 389 - 390
Linked Comment: Ultrasound Obstet Gynecol 2015; 46: 452–459 
Pregnancy | Fetal Growth Retardation - diagnostic imaging | Humans | Skull - abnormalities | Ultrasonography | Female | Male | Brain - abnormalities
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17. Full Text Abnormality on a skull radiograph
by Tan, Janice Ser Huey and Tan, Timothy Shao Ern
BMJ, ISSN 0959-8146, 1/2017, Volume 356, p. i6315
MEDICINE, GENERAL & INTERNAL | Multiple Myeloma - diagnostic imaging | Female | Aged | Humans | Fatal Outcome | Skull Neoplasms - diagnostic imaging
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18. Full Text CT Reveals a High Incidence of Osseous Abnormalities in Hips with Labral Tears
by Dolan, Mark M and Heyworth, Benton E and Bedi, Asheesh and Duke, Gavin and Kelly, Bryan T
Clinical Orthopaedics and Related Research, ISSN 0009-921X, 3/2011, Volume 469, Issue 3, pp. 831 - 838
Acetabular labral tears are being diagnosed with increasing frequency and there is a growing consensus that these tears rarely occur in the absence of osseous... 
Surgical Orthopedics | Medicine & Public Health | Sports Medicine | Surgery | Orthopedics | Conservative Orthopedics | Medicine/Public Health, general | EPIPHYSIS | SURGERY | ANTEVERSION | YOUNG | FEMOROACETABULAR IMPINGEMENT | RETROVERSION | ARTHROSCOPY | RADIOGRAPHIC EVALUATION | OSTEOARTHRITIS | NECK | ORTHOPEDICS | FEMORO-ACETABULAR IMPINGEMENT | Humans | Acetabulum - injuries | Tomography, X-Ray Computed - methods | Femur - diagnostic imaging | Femur - abnormalities | Magnetic Resonance Imaging | Hip Injuries - diagnostic imaging | Cartilage, Articular - injuries | Hip Injuries - epidemiology | Rupture - epidemiology | Acetabulum - abnormalities | Acetabulum - diagnostic imaging | Michigan - epidemiology | Medical colleges | CT imaging | Diagnostic imaging | Orthopedic surgery | Health aspects | Femur | Computed tomography | Magnetic resonance imaging | Coxa | Acetabulum | Skull | Hip | Tears | Clinical Research
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19. Etiology-based dental and craniofacial diagnostics
by Kjær, Inger, author
2017, ISBN 9781118912102, xii, 244 pages
Etiology-Based Dental and Craniofacial Diagnostics explores the role of embryology and fetal pathology in the assessment, diagnosis, and subsequent treatment... 
Skull | Growth | Abnormalities | Teeth | Skull - embryology
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20. Full Text Spag17 deficiency results in skeletal malformations and bone abnormalities
by Teves, Maria Eugenia and Sundaresan, Gobalakrishnan and Cohen, David J and Hyzy, Sharon L and Kajan, Illya and Maczis, Melissa and Zhang, Zhibing and Costanzo, Richard M and Zweit, Jamal and Schwartz, Zvi and Boyan, Barbara D and Strauss, Jerome F
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, p. e0125936
Height is the result of many growth and development processes. Most of the genes associated with height are known to play a role in skeletal development.... 
PF6 | POPULATION | CELLS | COMPLEX | PATTERN | MULTIDISCIPLINARY SCIENCES | GROWTH-PLATE | LOCI | PRIMARY CILIUM | ADULT HEIGHT | CARTILAGE | Animals, Newborn | Chondrocytes - pathology | Skull - physiopathology | Cilia - pathology | Mice, Inbred C57BL | Cells, Cultured | Microtubule Proteins - metabolism | Male | Femur - abnormalities | Mice, Knockout | Osteoblasts - pathology | Tibia - abnormalities | Animals | Female | Microtubule Proteins - genetics | Bone and Bones - abnormalities | Osteoblasts - metabolism | Chondrocytes - metabolism | Bone and Bones - cytology | Care and treatment | Abnormalities | Bones | Development and progression | Genetic aspects | Single nucleotide polymorphisms | Research | Femur | Sperm | Biochemistry | Single-nucleotide polymorphism | Bone (trabecular) | Osteoblasts | Ossification | Defects | Morphogenesis | Proteins | Cartilage | Growth plate | Engineering | Bone growth | Biomedical materials | Tibia | Mineralization | Rodents | Fibroblasts | Extracellular matrix | Biocompatibility | Growth factors | Biomedical engineering | Cilia | Antigens | Osteocalcin | Gynecology | siRNA | Embryo fibroblasts | Embryos | Obstetrics | Mutants | Studies | Chondrocytes | Mice | Metacarpal | Bone | Molecular biology | Osteogenesis
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