Omphalocele in three generations with autosomal dominant transmission

Journal of Medical Genetics

Volumn 39, Issue 3, 2002, Pages 184-185

  Kanagawa, S L ^a   Begleiter, M L ^a   Ostlie, D J ^a   Holcomb, G ^a   Drake, W ^a   Butler, M G ^a  

^a UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC LINKAGE; HEREDITY; HUMAN; INFANT; INHERITANCE; KARYOTYPE; MALE; OMPHALOCELE; PRIORITY JOURNAL; TREATMENT PLANNING;

EID: 0036195406     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.39.3.184     Document Type: Article

References (7)

1. Familial occurrence of omphalocele suggesting sex-linked inheritance
2. Familial omphalocele: Considerations in genetic counseling
3. Four cases of omphalocele in two generations of the same family
4. Familial occurrence of omphalocele
5. Omphalocele in half siblings
6. Familial omphalocele