Duplication of 15q11.2-q14, including theP gene, in a woman with generalized skin hyperpigmentation
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. The genetics of pigmentation: from fancy genes to complex traits
2. Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations
3. Large genomic duplicons map to sites of instability in the Prader- Willi/Angelman syndrome chromosome region (15q11-q13)
4. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.
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3. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature;Molecular Cytogenetics;2018-02-05
4. Molecular Biology of Albinism;Albinism in Africa;2018
5. Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature;Cytogenetic and Genome Research;2016
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