Congenital Hypothyroidism in Young-Simpson Syndrome-Reference-Cited by-同舟云学术

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Congenital Hypothyroidism in Young-Simpson Syndrome

Published:2008-01 Issue:11 Volume:21 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Stagi S.,Bindi G.,Lapi E.,Giovannucci-Uzielli M.L.,Salti R.,Chiarelli F.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/JPEM.2008.21.11.1089/pdf

Reference14 articles.

1. Unknown syndrome: abnormal facies, congenital heart defects, hypothyroidism, and severe retardation.

2. Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.

3. Unknown syndrome: abnormal facies, hypothyroidism, postaxial polydactyly, and severe retardation: a third patient.

4. Parental consanguinity in the blepharophimosis, heart defect, hypothyroidism, mental retardation syndrome (Young-Simpson syndrome).

5. A Japanese boy with Young-Simpson syndrome

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. De novo mutations of the gene encoding the histone acetyltransferase KAT6B in two patients with Say-Barber/Biesecker/Young-Simpson syndrome;American Journal of Medical Genetics Part A;2013-02-22

2. Cutaneous Manifestations of Endocrine Disease;Harper's Textbook of Pediatric Dermatology;2011-05-24

3. Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11));Clinical Endocrinology;2009-10-26

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