Neural tube defects in Waardenburg syndrome: A case report and review of the literature

Author:

Hart Joseph1ORCID,Miriyala Kalpana1

Affiliation:

1. Joan C Edwards School of Medicine; Marshall University; Huntington West Virginia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference36 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nature Methods,2010

2. Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida;Agopian;Birth Defects Research Part A, Clinical and Molecular Teratology,2013

3. ACOG practice nulletin no. 101: Ultrasonography in pregnancy;Obstetrics and Gynecology,2009

4. Possible homozygous Waardenburg syndrome in a fetus with exencephaly;Aymé;American Journal of Medical Genetics,1995

5. Mutations in PAX3 that cause Waardenburg syndrome type I: Ten new mutations and review of the literature;Baldwin;American Journal of Medical Genetics,1995

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3