A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES

Authors
ROUSSEAU F HEITZ D TARLETON J MACPHERSON J PETTERSON U MATHEW C MORNET E MADDALENA A SCHINZEL A MARCOS JAG SCHORDERET DF SCHAAP T MACCIONI L RUSSO S JACOBS PA SCHWARTZ C MANDEL JL
Citation
F. Rousseau et al., A COLLABORATIVE MULTICENTER STUDY OF DIRECT DIAGNOSIS OF THE FRAGILE-X SYNDROME WITH PROBE STB12.3 - THE 1ST 2253 CASES, American journal of human genetics, 53(3), 1993, pp. 78-78
Citations number
NO
Categorie Soggetti
Genetics & Heredity
Journal title
American journal of human genetics → ACNP
ISSN journal
00029297
Volume
53
Issue
3
Year of publication
1993
Supplement
S
Pages
78 - 78
Database
ISI
SICI code
0002-9297(1993)53:3<78:ACMSOD>2.0.ZU;2-3