The Greig cephalopolysyndactyly syndrome

Orphanet Journal of Rare Diseases

Volumn 3, Issue 1, 2008, Pages

  Biesecker, Leslie G ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLI3 PROTEIN, HUMAN; KRUPPEL LIKE FACTOR; NERVE PROTEIN;

BRAIN; CONGENITAL MALFORMATION; DIFFERENTIAL DIAGNOSIS; GENETICS; HUMAN; HYPERTELORISM; MULTIPLE MALFORMATION SYNDROME; PRENATAL DIAGNOSIS; PROGNOSIS; RARE DISEASE; RECURRENT DISEASE; REVIEW; RISK FACTOR; SYNDACTYLY; SYNDROME;

ABNORMALITIES, MULTIPLE; BRAIN; DIAGNOSIS, DIFFERENTIAL; HUMANS; HYPERTELORISM; KRUPPEL-LIKE TRANSCRIPTION FACTORS; NERVE TISSUE PROTEINS; PRENATAL DIAGNOSIS; PROGNOSIS; RARE DISEASES; RECURRENCE; RISK FACTORS; SYNDACTYLY; SYNDROME;

EID: 44449129420     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-3-10     Document Type: Article

References (26)

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