Exclusion of MYF5, GSC, RUNX2, and TCOF1 mutation in a case of cerebro-costo-mandibular syndrome

Clinical Dysmorphology

Volumn 19, Issue 2, 2010, Pages 51-55

  Su, Pen Hua ^a,b   Chen, Jia Yuh ^a,b   Chiang, Chin Lung ^a   Ng, Yan Yan ^a   Chen, Suh Jen ^a  

^a CHUNG SHAN MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^b CHUNG SHAN MEDICAL UNIVERSITY   (Taiwan)

Author keywords

Cerebro costo mandibular syndrome; Comparative genome hybridization; GSC gene; MYF5 gene; RUNX2 gene; TCOF1 gene

Indexed keywords

GOOSECOID PROTEIN; MYOGENIC FACTOR 5; TRANSCRIPTION FACTOR RUNX2;

ARTICLE; CASE REPORT; CEREBRO COSTO MANDIBULAR SYNDROME; CHROMOSOME ANALYSIS; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL MALFORMATION; FETUS ECHOGRAPHY; GENE; GENE MUTATION; HUMAN; LARYNGEAL MASK; MALE; MICROGNATHIA; NEWBORN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; THORAX RADIOGRAPHY; THREE DIMENSIONAL IMAGING; TREACHER COLLINS FRANCESCHETTI SYNDROME 1 GENE;

ABNORMALITIES, MULTIPLE; ADULT; CORE BINDING FACTOR ALPHA 1 SUBUNIT; CRANIOFACIAL ABNORMALITIES; FEMALE; GOOSECOID PROTEIN; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; MYOGENIC REGULATORY FACTOR 5; NUCLEAR PROTEINS; PHOSPHOPROTEINS; PREGNANCY; RADIOGRAPHY, THORACIC; SKULL; SYNDROME;

EID: 77949376134     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e328335c133     Document Type: Article

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