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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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P N Schofield

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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.

The Journal of Pathology|November 20, 2008

An impending crisis in the provision of histopathology expertise for mouse functional genomicsM V Warren, M L Studley, P Dubus, et al.

International Journal of Radiation Biology|November 19, 2008

Progress in updating the European Radiobiology ArchivesS Tapio, P N Schofield, C Adelmann, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.

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Search research articles

Showing results (71-80 of 74) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 74 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.

The Journal of Pathology|November 20, 2008

An impending crisis in the provision of histopathology expertise for mouse functional genomicsM V Warren, M L Studley, P Dubus, et al.

International Journal of Radiation Biology|November 19, 2008

Progress in updating the European Radiobiology ArchivesS Tapio, P N Schofield, C Adelmann, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.

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