DNA deletion and its parental origin in Angelman syndrome patients
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference16 articles.
1. PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROME
2. Report of the committee on the genetic constitution of chromosomes 14 and 15
3. Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes
4. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within thePWCR
5. Styl polymorphism at the D15S11 locus
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