THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM (OCA2), AND HYPOPIGMENTATION IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME

Citation
Mh. Brilliant et al., THE MOUSE PINK-EYED DILUTION GENE - ASSOCIATION WITH HUMAN TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM (OCA2), AND HYPOPIGMENTATION IN PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME, American journal of human genetics, 53(3), 1993, pp. 161-161
Citations number
NO
Categorie Soggetti
Genetics & Heredity
ISSN journal
00029297
Volume
53
Issue
3
Year of publication
1993
Supplement
S
Pages
161 - 161
Database
ISI
SICI code
0002-9297(1993)53:3<161:TMPDG->2.0.ZU;2-X