Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of theP gene
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference20 articles.
1. Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints
2. Large genomic duplicons map to sites of instability in the Prader- Willi/Angelman syndrome chromosome region (15q11-q13)
3. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism
4. Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African‐Americans
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