PRENATAL-DIAGNOSIS AND CARRIER DETECTION FOR A POINT MUTATION IN UBE3A CAUSING ANGELMAN-SYNDROME

Authors
TSAI TF RAASROTHSCHILD A BENNERIAH Z BEAUDET AL
Citation
Tf. Tsai et al., PRENATAL-DIAGNOSIS AND CARRIER DETECTION FOR A POINT MUTATION IN UBE3A CAUSING ANGELMAN-SYNDROME, American journal of human genetics, 63(5), 1998, pp. 1561-1563
Citations number
11
Categorie Soggetti
Genetics & Heredity
Journal title
American journal of human genetics → ACNP
ISSN journal
00029297
Volume
63
Issue
5
Year of publication
1998
Pages
1561 - 1563
Database
ISI
SICI code
0002-9297(1998)63:5<1561:PACDFA>2.0.ZU;2-K