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Journal of Medical Genetics|July 29, 1999

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.

Human Molecular Genetics|March 11, 1999

Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancerF M Richards, S A McKee, M H Rajpar, et al.

Journal of Medical Genetics|February 5, 2008

Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardationR H Scott, J Douglas, L Baskcomb, et al.

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You have reached the last page of results.This site can display upto 23 results.

Journal of Medical Genetics|July 29, 1999

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.

Human Molecular Genetics|March 11, 1999

Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancerF M Richards, S A McKee, M H Rajpar, et al.

Journal of Medical Genetics|February 5, 2008

Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardationR H Scott, J Douglas, L Baskcomb, et al.

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