Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability-Reference-Cited by-同舟云学术

Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability

Published:2011-11-21 Issue:1 Volume:158A Page:159-165
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Millson Alison,LaGrave Danielle,Willis Mary J.H.,Rowe Leslie R.,Lyon Elaine,South Sarah T.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34349/fullpdf

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3. An emerging 1q21.1 deletion-associated neurodevelopmental phenotype;Basel-Vanagaite;J Child Neurol,2011

4. Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2;Chubykin;Neuron,2007

5. A copy number variation morbidity map of developmental delay;Cooper;Nat Genet,2011

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