Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, the Netherlands. I: Syndromes with multiple congenital anomalies

American Journal of Medical Genetics

Volumn 77, Issue 2, 1998, Pages 100-115

  Oostra, Roelof Jan ^a   Baljet, Bob ^a   Dijkstra, Piet F ^a   Hennekam, Raoul C M ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

Acrofacial dysostosis; Anatomical specimen; Apert syndrome; Brachmann De Lange syndrome; Ichthyosis congenita gravis; Jarcho Levin syndrome; Meckel syndrome; Multiple congenital anomalies; Oro facio digital syndrome; Roberts syndrome; Smith Lemli Opitz syndrome; Teratology; Treacher Collins syndrome; Trisomy 13; Vrolik

Indexed keywords

ACROCEPHALOSYNDACTYLY; ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; CONGENITAL MALFORMATION; CONTROLLED STUDY; DE LANGE SYNDROME; DYSOSTOSIS; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; INFANT; JARCHO LEVIN SYNDROME; MALE; MANDIBULOFACIAL DYSOSTOSIS; MECKEL SYNDROME; NETHERLANDS; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; ROBERTS SYNDROME; SMITH LEMLI OPITZ SYNDROME; SYNDROME; TERATOLOGY; TRISOMY 13;

ABNORMALITIES, MULTIPLE; FEMALE; FETUS; HISTORY, 18TH CENTURY; HISTORY, 19TH CENTURY; HUMANS; MALE; MUSEUMS; NETHERLANDS; SYNDROME; TERATOLOGY;

EID: 0032079382     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980501)77:2<100::AID-AJMG3>3.0.CO;2-W     Document Type: Article

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