Candidate region for cardio-facio-cutaneous syndrome [1]

American Journal of Medical Genetics

Volumn 101, Issue 2, 2001, Pages 173-

  Rauen, Katherine A ^a,b   Cotter, Philip D ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b CHILDREN S HOSPITAL OAKLAND   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARDIOFACIOCUTANEOUS SYNDROME; CHROMOSOME 12Q; CHROMOSOME BAND; CHROMOSOME DELETION; CHROMOSOME PAINTING; CONGENITAL HEART DISEASE; FACE MALFORMATION; GENE LOCUS; HUMAN; HYBRIDIZATION; LETTER; PHENOTYPE; PRIORITY JOURNAL; SKIN DISEASE;

ABNORMALITIES, MULTIPLE; CARDIOVASCULAR ABNORMALITIES; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 12; CRANIOFACIAL ABNORMALITIES; HUMANS; SKIN ABNORMALITIES; SYNDROME;

EID: 0035877217     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1251     Document Type: Letter

References (3)

1. Cardio-facio-cutaneous (CFC) syndrome phenotype in an individual with an interstitial deletion of 12q: Identification of a candidate region for CFC syndrome
2. Mendelian cytogenetics. Chromosome rearrangements associated with Mendelian disorders
3. Letter to the editor - Partial deletion of chromosome 12q is not usually associated with CFC syndrome