ANALYSIS OF GERMLINE P57(KIP2) 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., ANALYSIS OF GERMLINE P57(KIP2) MUTATIONS IN THE HUMAN IMPRINTING DISORDER - BECKWITH-WIEDEMANN-SYNDROME (BWS) PROVIDES A NOVEL GENOTYPE-PHENOTYPE CORRELATION, Journal of Medical Genetics, 34, 1997, pp. 38-38
Citations number
NO
Categorie Soggetti
Genetics & Heredity
Journal title
Journal of Medical Genetics → ACNP
ISSN journal
00222593
Volume
34
Year of publication
1997
Supplement
1
Pages
38 - 38
Database
ISI
SICI code
0022-2593(1997)34:<38:AOGPMI>2.0.ZU;2-A