AN INSERTION DELETION POLYMORPHISM AT THE D15S63 LOCUS IN THE CRITICAL PRADER-WILLI-SYNDROME REGION IN 15Q11-13/
Citation
B. Dittrich et al., AN INSERTION DELETION POLYMORPHISM AT THE D15S63 LOCUS IN THE CRITICAL PRADER-WILLI-SYNDROME REGION IN 15Q11-13/, Human genetics, 94(5), 1994, pp. 583-584
Categorie Soggetti
Genetics & Heredity
SICI code
0340-6717(1994)94:5<583:AIDPAT>2.0.ZU;2-L
Abstract
The probe YR9AB detects a two-allele insertion/deletion polymorphism a
t the D15S63 locus.