Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review-Reference-Cited by-同舟云学术

Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review

Published:2019-11-11 Issue:2 Volume:84 Page:169-176
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Annals of Human Genetics

Author:

Yuan Meizhen¹,Deng Linbei¹,Yang Yingjun¹,Sun Luming¹

Affiliation:

1. Department of Fetal Medicine and Prenatal Diagnosis Center, Shanghai First Maternity and Infant Hospital Tongji University School of Medicine Shanghai China

Funder

Shanghai municipal medical and health discipline

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12360

Reference45 articles.

1. Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y

2. Williams syndrome.

3. Action of TFII-I Outside the Nucleus as an Inhibitor of Agonist-Induced Calcium Entry

4. The contribution of GTF2I haploinsufficiency to Williams syndrome

5. High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions

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