Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity-Reference-Cited by-同舟云学术

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Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

Published:2010-10 Issue:10 Volume:12 Page:641-647
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Bachmann-Gagescu Ruxandra,Mefford Heather C.,Cowan Charles,Glew Gwen M.,Hing Anne V.,Wallace Stephanie,Bader Patricia I.,Hamati Aline,Reitnauer Pamela J.,Smith Rosemarie,Stockton David W.,Muhle Hiltrud,Helbig Ingo,Eichler Evan E.,Ballif Blake C.,Rosenfeld Jill,Tsuchiya Karen D.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference36 articles.

Cited by 171 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. The Phenotypic Spectrum of 16p11.2 Recurrent Chromosomal Rearrangements;Genes;2024-08-10

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

3. The Association between Obesity Susceptibility and Polymorphisms of MC4R, SH2B1, and NEGR1 in Tibetans;Genetic Testing and Molecular Biomarkers;2024-07-01

4. SH2B1 Defends Against Energy Imbalance, Obesity, and Metabolic Disease via a Paraventricular Hypothalamus→Dorsal Raphe Nucleus Neurocircuit;Advanced Science;2024-06-17

5. Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes;The Journal of Clinical Endocrinology & Metabolism;2024-05-08

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