POINT MUTATION IN INTRON-10 OF FMR1 IS UNLIKELY TO BE A CAUSE OF FRAGILE-X-SYNDROME

Authors
VINCENT JB GURLING HMD
Citation
Jb. Vincent et Hmd. Gurling, POINT MUTATION IN INTRON-10 OF FMR1 IS UNLIKELY TO BE A CAUSE OF FRAGILE-X-SYNDROME, Human mutation, 12(6), 1998, pp. 431-431
Citations number
4
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Volume
12
Issue
6
Year of publication
1998
Pages
431 - 431
Database
ISI
SICI code
1059-7794(1998)12:6<431:PMIIOF>2.0.ZU;2-P