WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion-Reference-Cited by-同舟云学术

WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion

Published:2017-04-11 Issue:6 Volume:173 Page:1690-1693
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Huynh Minh Tuan¹²³^ORCID,Boudry-Labis Elise¹,Duban Bénédicte⁴,Andrieux Joris¹,Tran Cong Toai²,Tampere Heidi¹,Ceraso Delphine¹,Manouvrier Sylvie⁵,Tachdjian Gérard³,Roche-Lestienne Catherine¹,Vincent-Delorme Catherine⁵

Affiliation:

1. Institut de Génétique Médicale et Université de Lille 2; Hôpital Jeanne de Flandre; Lille France

2. Pham Ngoc Thach Medical University; Ho Chi Minh city Vietnam

3. Service d'Histologie Embryologie et Cytogénétique; Hôpitaux Universitaires Paris Sud; SiteAntoine Béclère, APHP; Clamart France

4. Centre de Cytogénétique; Hôpital Saint Vincent de Paul; Lille France

5. Service de Génétique Clinique Guy Fontaine et Université de Lille 2; Hôpital Jeanne de Flandre; Lille France

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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3. A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis;Baris;Clinical Journal of Endocrinology and Metabolism,2006

4. Association of FOXE1 polyalanine repeat region with papillary thyroid cancer;Bullock;The Journal of Clinical Endocrinology and Metabolism,2012

5. Polymorphic length of FOXE1 alanine stretch: Evidence for genetic susceptibility to thyroid dysgenesis;Carré;Human Genetics,2007

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5. Prevalence of mosaicism in uncultured chorionic villus samples after chromosomal microarray and clinical outcome in pregnancies affected by confined placental mosaicism;Prenatal Diagnosis;2019-11-26