Familial occurrence of omphalocele suggesting sex-linked inheritance.-Reference-Cited by-同舟云学术

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Familial occurrence of omphalocele suggesting sex-linked inheritance.

Published:1979-02-01 Issue:2 Volume:54 Page:142-143
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Havalad S,Noblett H,Speidel B D

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Exomphalos with macroglossia. A study of eleven cases;Irving, I.M.;Journal ofPediatric Surgery,1967

2. An investigation of 69 cases of exomphalos;McKeown, T.B.; MacMohan, B.; Record, R.G.;American Journal of Genetics,1953

3. Four cases of omphalocele in two generations of the same family;Osuna, A.; Lindham, S.;Clinical Genetics,1976

4. Omphalocele in siblings. Report of two cases with surgical recovery;Rothemberg, R.E.; Barnet, T.;Archives of Surgery,1974

5. Familial occurrence of omphalocele;Rott, H.D.; Truckenbrodt, L.H.;Humangenetik,1974

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1. Prenatal Diagnosis and Management of Abnormal Fetal Development in the Third Trimester of Pregnancy;Genetic Disorders and the Fetus;2021-04-20

2. Omphalocele: a review of common genetic etiologies;Egyptian Journal of Medical Human Genetics;2019-12

3. Omphalocele;Atlas of Genetic Diagnosis and Counseling;2017

4. Congenital omphalocele and cleft palate in two fetuses;Congenital Anomalies;2016-07

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