W syndrome: Report of three cases and review

American Journal of Medical Genetics

Volumn 87, Issue 5, 1999, Pages 446-449

  Goizet, Cyril ^a   Bonneau, Dominique ^b   Lacombe, Didier ^a  

^a HÔPITAL PELLEGRIN   (France)

^b POITIERS UNIVERSITY HOSPITAL   (France)

Author keywords

Facial anomalies; Short stature; Spasticity; W syndrome; X linked dominant inheritance; X linked mental retardation

Indexed keywords

ARTICLE; CASE REPORT; FACE MALFORMATION; FAMILY HISTORY; HUMAN; INFANT; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MULTIPLE MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SEIZURE; SPASTICITY; X CHROMOSOME DOMINANT DISORDER;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; BONE AND BONES; CHILD; CLEFT LIP; CLEFT PALATE; DEVELOPMENTAL DISABILITIES; FACIES; GENES, DOMINANT; HUMANS; MALE; MENTAL RETARDATION; PHENOTYPE; SYNDROME; TOOTH ABNORMALITIES; X CHROMOSOME;

EID: 0033407103     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991222)87:5<446::AID-AJMG15>3.0.CO;2-F     Document Type: Article

References (5)

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