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Article

Developmental disability and hypomelanosis of Ito in a female with 7.3 Mb de novo duplication of Xp11.3-p11.4 and random X inactivation.

American journal of medical genetics. Part A - 1 Nov 2009

Zou Ying S, Milunsky Jeff M

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Share to Base Pairing
Share to Chromosome Banding
Share to Chromosomes, Human, X
Share to Developmental Disabilities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Duplication

Share to Hypopigmentation

Share to Intellectual Disability

Share to X Chromosome Inactivation

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Identifiers

PMID: 19876908
DOI: 10.1002/ajmg.a.33066

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