Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: A new X-linked dominant multiple congenital anomalies syndrome?

American Journal of Medical Genetics

Volumn 90, Issue 5, 2000, Pages 351-355

  Manouvrier, Sylvie ^a   Moerman, Alexandre ^a   Coeslier, Anne ^a   Devisme, L ^a   Boute, Odile ^a   Le Merrer, Martine ^b  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Radial ray; X linked dominant; XK aprosencephaly

Indexed keywords

ADULT; ARTICLE; CLINICAL FEATURE; DIAGNOSTIC IMAGING; FEMALE; FETUS; HUMAN; KARYOTYPING; MALE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; RADIODIAGNOSIS; SPONTANEOUS ABORTION; SYNDROME; SYNOSTOSIS; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; ABORTION, SPONTANEOUS; ADULT; FEMALE; FETUS; HUMANS; MALE; PEDIGREE; PREGNANCY; RADIUS; SYNDACTYLY; SYNDROME; SYNOSTOSIS; ULNA; X CHROMOSOME;

EID: 0034723736     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000228)90:5<351::AID-AJMG1>3.0.CO;2-K     Document Type: Article

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