Coffin-Siris syndrome: Review and presentation of new cases from a questionnaire study

American Journal of Medical Genetics

Volumn 99, Issue 1, 2001, Pages 1-7

  Fleck, Barbara J ^a,b   Pandya, Arti ^a   Vanner, Lauren ^a   Kerkering, Kathryn ^a   Bodurtha, Joann ^a  

^a VIRGINIA COMMONWEALTH UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL OF THE KING S DAUGHTERS   (United States)

Author keywords

Clinical morphology; Delineation of disease; Natural history

Indexed keywords

ADOLESCENT; ADULT; BONE MALFORMATION; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COFFIN SIRIS SYNDROME; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; HIRSUTISM; HUMAN; HYPOPLASIA; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; REVIEW; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; FACE; FEMALE; HUMANS; INFANT; MALE; MENTAL RETARDATION; QUESTIONNAIRES; SYNDROME;

EID: 0035866023     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010215)99:1<1::AID-AJMG1127>3.0.CO;2-A     Document Type: Review

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