The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review
Author:
Funder
NICHD
Publisher
MDPI AG
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis
Link
http://www.mdpi.com/1422-0067/16/2/4068/pdf
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2. Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons
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4. Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome
5. Behavioral Differences Among Subjects With Prader-Willi Syndrome and Type I or Type II Deletion and Maternal Disomy
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