Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis-Reference-Cited by-同舟云学术

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Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis

Published:2008 Issue:9 Volume:146A Page:1117-1127
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kulkarni Shashikant,Nagarajan Prabakaran,Wall Jonathan,Donovan Diana J.,Donell Robert L.,Ligon Azra H.,Venkatachalam Sundaresan,Quade Bradley J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference54 articles.

1. SNTG1, the gene encoding ?1-syntrophin: a candidate gene for idiopathic scoliosis

2. Good genes in bad neighbourhoods

3. De novo t(2;13)(p24.3;q14.2) and retinoblastoma

4. Multiple mutations in mouse Chd7 provide models for CHARGE syndrome

5. Mi-2/NuRD: multiple complexes for many purposes

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2. Effects of two chd2-knockout strains on the morphology and behavior in zebrafish;Development Genes and Evolution;2024-08-27

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4. Chromatin gatekeeper and modifier CHD proteins in development, and in autism and other neurological disorders;Psychiatric Genetics;2023-10-16

5. Rise of the Chromodomain Helicase DNA‐Binding (CHD) Chromatin Remodelling Machines;Encyclopedia of Life Sciences;2023-03-30

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