TCF2/HNF-1beta mutations: 3 cases of fetal severe pancreatic agenesis or hypoplasia and multicystic renal dysplasia-Reference-Cited by-同舟云学术

TCF2/HNF-1beta mutations: 3 cases of fetal severe pancreatic agenesis or hypoplasia and multicystic renal dysplasia

Published:2014-01 Issue:1 Volume:34 Page:90-93
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Body-Bechou Delphine¹,Loget Philippe²,D'Herve Dominique³,Le Fiblec Bernard⁴,Grebille Anne-Gaelle⁴,Le Guern Hélène⁵,Labarthe Caroline⁶,Redpath Margaret⁷,Cabaret-Dufour Anne-Sophie¹,Sylvie Odent⁸,Fievet Alice⁸,Antignac Corinne⁹,Heidet Laurence¹⁰,Taque Sophie¹¹,Patrice Poulain¹

Affiliation:

1. Obstetrics and Gynecology; CHU Rennes; Rennes France

2. Pathology laboratory; CHU Rennes; Rennes France

3. Ultrasound; Clinique Mutualiste de la Sagesse; Rennes France

4. Gynécologie-obstétrique; CH Yves Le Foll; Saint-Brieuc France

5. Obstetrics; CH Saint Brieuc; Saint Brieuc France

6. Obstetrics; CHP Saint Grégoire; Saint Grégoire France

7. Lady Davis Institut, Jewish General Hospital; McGill University; Montreal Quebec Canada

8. Clinical Genetics; CHU Rennes; CHU Rennes; Rennes France

9. Genetics; Hôpital Necker; Paris France

10. Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte, Pediatric Nephrology; AP-HP, Necker-Enfants Malades Hospital; Paris France

11. Pediatrics; CHU Rennes; Rennes France

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference7 articles.

1. Lack of TCF2/vHNF1 in mice leads to pancreas agenesis;Haumaitre;Proc Natl Acad Sci U S A,2005

2. Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases;Heidet;Clin J Am Soc Nephrol: CJASN,2010

3. Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes;Madariaga;Clin J Am Soc Nephrol: CJASN,2013

4. Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys;Decramer;Clin J Am Soc Nephrol: JASN,2007

5. GATA6 haploinsufficiency causes pancreatic agenesis in humans;Allen;Nat Genet,2012

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