AAAAAA

   
Results: 1-4 |
Results: 4
BECKWITH-WIEDEMANN-SYNDROME IN A CHILD WITH CHROMOSOME 18Q DELETION
Authors: BREWER CM LAM WWK HAYWARD C GRACE E MAHER ER FITZPATRICK DR
Citation: Cm. Brewer et al., BECKWITH-WIEDEMANN-SYNDROME IN A CHILD WITH CHROMOSOME 18Q DELETION, Journal of Medical Genetics, 35(2), 1998, pp. 162-164
EPIGENETIC MODIFICATION AND UNIPARENTAL INHERITANCE OF H19 IN BECKWITH-WIEDEMANN-SYNDROME
Authors: CATCHPOOLE D LAM WWK VALLER D TEMPLE IK JOYCE JA REIK W SCHOFIELD PN MAHER ER
Citation: D. Catchpoole et al., EPIGENETIC MODIFICATION AND UNIPARENTAL INHERITANCE OF H19 IN BECKWITH-WIEDEMANN-SYNDROME, Journal of Medical Genetics, 34(5), 1997, pp. 353-359
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
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
Risultati: 1-4 |