Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations-Reference-Cited by-同舟云学术

Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations

Published:2010-10 Issue:4 Volume:203 Page:364.e1-364.e5
ISSN:0002-9378
Container-title:American Journal of Obstetrics and Gynecology
language:en
Short-container-title:American Journal of Obstetrics and Gynecology

Author:

Oram Richard A.,Edghill Emma L.,Blackman Jenny,Taylor Miles J.O.,Kay Tracey,Flanagan Sarah E.,Ismail-Pratt Ida,Creighton Sarah M.,Ellard Sian,Hattersley Andrew T.,Bingham Coralie

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference21 articles.

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3. The preterm prediction study: risk factors for indicated preterm births: Maternal-Fetal Medicine Units Network of the National Institute of Child Health and Human Development;Meis;Am J Obstet Gynecol,1998

4. Familial bilateral renal agenesis and hereditary renal adysplasia;Buchta;Z Kinderheilkd,1973

5. Hereditary urogenital adysplasia;Schimke;Clin Genet,1980

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