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greig cephalopolysyndactyly syndrome (118) 118
humans (107) 107
genetics & heredity (82) 82
animals (79) 79
zinc finger protein gli3 (58) 58
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polydactyly (34) 34
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abnormalities, multiple - genetics (32) 32
kruppel-like transcription factors - genetics (32) 32
developmental biology (31) 31
greig syndrome (31) 31
polydactyly - genetics (31) 31
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deletion (24) 24
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hedgehog proteins (23) 23
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sonic hedgehog (22) 22
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expression (21) 21
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cell biology (20) 20
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genetic aspects (18) 18
mutations (17) 17
pallister-hall syndrome (17) 17
point mutations (17) 17
acrocephalosyndactylia - genetics (16) 16
limb development (16) 16
molecular sequence data (16) 16
syndactyly - genetics (16) 16
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chromosomes, human, pair 7 (13) 13
craniosynostosis (13) 13
dna-binding proteins - metabolism (13) 13
genetics (13) 13
greig cephalopolysyndactyly (13) 13
infant, newborn (13) 13
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Genetic Testing and Molecular Biomarkers, ISSN 1945-0265, 10/2019, Volume 23, Issue 10, pp. 744 - 750
Background: Greig cephalopolysyndactyly syndrome (GCPS) is a disorder of autopod and craniofacial abnormalities. Autopod anomalies include preaxial and/or... 
Genetic counseling | Greig cephalopolysyndactyly syndrome | Abnormalities | Polydactyly | Syndactyly | Gli3 protein | Genetic screening | Anomalies
Journal Article
Journal of medical case reports, ISSN 1752-1947, 04/2019, Volume 13, Issue 1, pp. 100 - 5
Greig cephalopolysyndactyly syndrome is a rare multiple congenital anomaly syndrome characterized by the triad of polysyndactyly (preaxial or mixed preaxial... 
Genetic aspects | Research | Greig cephalopolysyndactyly syndrome | Comorbidity | Autism | Genotype & phenotype | Genetic counseling | Sleep | Social research | Intellectual disabilities | Behavior | Quantitative psychology | Mutation | Age | Child & adolescent psychiatry | Development | Neuropsychological phenotype | Intellectual disability
Journal Article
Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology, ISSN 2212-5558, 09/2019, Volume 31, Issue 5, pp. 327 - 332
Typical Greig cephalopolysyndactyly syndrome (GCPS) is characterized by preaxial polydactyly or mixed pre- and postaxial polydactyly, true widely spaced eyes,... 
Orthognathic surgery | Greig syndrome | Double jaw surgery
Journal Article
Diagnostic Pathology, ISSN 1746-1596, 01/2018, Volume 13, Issue 1
A proper balance between the activator and the repressor form of GLI3, a zinc-finger transcription factor downstream of hedgehog signaling, is essential for... 
Case studies | Agenesis | Care and treatment | Gene mutations | Greig cephalopolysyndactyly syndrome | Physiological aspects | Genetic aspects | Diagnosis | Pallister-Hall syndrome
Journal Article
ANALES DE PEDIATRIA, ISSN 1695-4033, 04/2011, Volume 74, Issue 4, pp. 266 - 269
Greig cephalopolysyndactyly is a rare autosomic dominant syndrome caused by mutations in GLI3 gene located on cytoband 7p14.1 and characterized by the clinical... 
Array-CGH | GENE | Greig syndrome | PHENOTYPE | PEDIATRICS | 7p14.1 microdeletion | GLI3 | Chromosome Deletion | Phenotype | Humans | Female | Acrocephalosyndactylia - genetics | Chromosomes, Human, Pair 7 - genetics | Infant, Newborn
Journal Article
Reference
Journal Article
Acta Paediatrica Taiwanica, ISSN 1608-8115, 03/2006, Volume 47, Issue 2, pp. 95 - 99
We report on two cases (daughter and father) with Greig cephalopolysyndactyly syndrome (GCPS). The clinical manifestations in craniofacial structure, hands and... 
Multiple linkage analysis | Greig cephalopolysyndactyly syndrome | Preaxial polydactyly | Postaxial polydactyly | Polydactyly - genetics | Humans | Adult | Family | Female | Infant | Male | Hypertelorism - etiology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Syndrome | Genetic Linkage
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2003, Volume 120A, Issue 1, pp. 49 - 58
Journal Article
Annals of Plastic Surgery, ISSN 0148-7043, 05/2019, Volume 82, Issue 5, pp. 570 - 573
BACKGROUNDGLI3 encodes a transcription factor in the sonic hedgehog signaling pathway, which is essential in regulating the human limb bud development,... 
SURGERY | SONIC HEDGEHOG | isolated | PHENOTYPE | GLI3 | MOLECULAR ANALYSIS | mutation | LIMB DEVELOPMENT | GENE | syndrome | postpolydactyly | SPECTRUM | GREIG CEPHALOPOLYSYNDACTYLY SYNDROME | Gene mutations | Polydactyly | Causes of | Genetic aspects | Zinc finger proteins | Identification and classification | Health aspects
Journal Article
DEVELOPMENT, ISSN 0950-1991, 08/2014, Volume 141, Issue 15, pp. 3003 - 3012
talpid(2) is an avian autosomal recessive mutant with a myriad of congenital malformations, including polydactyly and facial clefting. Although phenotypically... 
Primary cilia | MOUSE | Gli processing | Ciliopathies | Hedgehog signaling | DEVELOPMENTAL BIOLOGY | TALPID3 MUTANT | GENE | CHICKEN EMBRYOS | DEVELOPMENTAL ABNORMALITIES | talpid | GLI PROTEINS | EXTRA-TOES | Craniofacial | Chicken | REPRESSOR FUNCTIONS | GREIG CEPHALOPOLYSYNDACTYLY SYNDROME
Journal Article
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