GERMLINE CDKNIC (P57KIP2) MUTATIONS IN THE HUMAN IMPRINTING DISORDER - BECKWITH-WIEDEMANN-SYNDROME (BWS) PROVIDES A NOVEL GENOTYPE-PHENOTYPE CORRELATION

Authors
LAM WWK HATADA I OHISHI S MUKAI T JOYCE JA COLE TRP REIK W SCHOFIELD PN MAHER ER
Citation
Wwk. Lam et al., GERMLINE CDKNIC (P57KIP2) MUTATIONS IN THE HUMAN IMPRINTING DISORDER - BECKWITH-WIEDEMANN-SYNDROME (BWS) PROVIDES A NOVEL GENOTYPE-PHENOTYPE CORRELATION, American journal of human genetics, 61(4), 1997, pp. 3-3
Citations number
NO
Journal title
American journal of human genetics → ACNP
ISSN journal
00029297
Volume
61
Issue
4
Year of publication
1997
Supplement
S
Pages
3 - 3
Database
ISI
SICI code
0002-9297(1997)61:4<3:GC(MIT>2.0.ZU;2-N