Interstitial 1q21.1 Microdeletion Is Associated with Severe Skeletal Anomalies, Dysmorphic Face and Moderate Intellectual Disability-Reference-Cited by-同舟云学术

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Interstitial 1q21.1 Microdeletion Is Associated with Severe Skeletal Anomalies, Dysmorphic Face and Moderate Intellectual Disability

Published:2016 Issue:6 Volume:7 Page:344-348
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Gamba Bruno F.,Zechi-Ceide Roseli M.,Kokitsu-Nakata Nancy M.,Vendramini-Pittoli Siulan,Rosenberg Carla,Krepischi Santos Ana C.V.,Ribeiro-Bicudo Lucilene,Richieri-Costa Antonio

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 20 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. Compound Point Mutation and Chromosomal Microdeletion Involving 1q21.1 Coinciding with ZMIZ1Variant:Newborns with Feeding Difficulties;2023-11-21

2. Phenotypic and genotypic characterization of 1q21.1 copy number variants: A report of 34 new individuals and literature review;American Journal of Medical Genetics Part A;2023-10-26

3. Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes;The American Journal of Human Genetics;2023-01

4. Isobaric Tags for Relative and Absolute Quantitation Identification of Blood Proteins Relevant to Paroxetine Response in Patients With Major Depressive Disorder;Frontiers in Psychiatry;2022-04-18

5. The Physiological Roles of the Exon Junction Complex in Development and Diseases;Cells;2022-04-01

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