FLUORESCENT IN-SITU HYBRIDIZATION FOR DIAGNOSIS OF PRADER-WILLI ANGELMAN SYNDROME

Authors
WENGER SL CUMMINS JH
Citation
Sl. Wenger et Jh. Cummins, FLUORESCENT IN-SITU HYBRIDIZATION FOR DIAGNOSIS OF PRADER-WILLI ANGELMAN SYNDROME, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 115-115
Citations number
NO
Categorie Soggetti
Cell Biology","Genetics & Heredity
Journal title
Cytogenetics and cell genetics → ACNP
ISSN journal
03010171
Volume
69
Issue
1-2
Year of publication
1995
Pages
115 - 115
Database
ISI
SICI code
0301-0171(1995)69:1-2<115:FIHFDO>2.0.ZU;2-M