Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis-Reference-Cited by-同舟云学术

Prenatal prevalence and postnatal manifestations of 16p11.2 deletions: A new insights into neurodevelopmental disorders based on clinical investigations combined with multi-omics analysis

Published:2024-01 Issue: Volume:552 Page:117671
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Liu Lan,Wang Jiamin,Liu Xijing,Wang Jing,Chen Lin,Zhu Hongmei,Mai Jingqun,Hu Ting,Liu Shanling

Funder

Sichuan Province Science and Technology Support Program

National Natural Science Foundation of China

Key Technologies Research and Development Program

National Key Research and Development Program of China

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Tibet Autonomous Region

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference44 articles.

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3. Recurrent 16p11.2 microdeletions in autism;Kumar;Hum. Mol. Genet.,2008

4. Simons Variation in Individuals Project, The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population;Hanson;Biol. Psychiatry,2015

5. Estimates of penetrance for recurrent pathogenic copy-number variations;Rosenfeld;Genet. Med.,2013

Cited by 2 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. Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication;BMC Pregnancy and Childbirth;2024-07-22

2. Concurrent of compound heterozygous variant of a novel in-frame deletion and the common hypomorphic haplotype in TBX6 and inherited 17q12 microdeletion in a fetus;BMC Pregnancy and Childbirth;2024-07-01