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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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J A Joyce

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Journal of Medical Genetics|May 1, 1997

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.

Journal of Medical Genetics|December 1, 1996

Microsatellite instability in early onset and familial colorectal cancerC Brassett, J A Joyce, N J Froggatt, et al.

Journal of Medical Genetics|April 25, 2000

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndromeD Catchpoole, A V Smallwood, J A Joyce, et al.

Oncogene|May 7, 2013

Heparanase promotes lymphangiogenesis and tumor invasion in pancreatic neuroendocrine tumorsK E Hunter, C Palermo, J C Kester, et al.

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.

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 (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

Journal of Medical Genetics|May 1, 1997

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndromeD Catchpoole, W W Lam, D Valler, et al.

Journal of Medical Genetics|December 1, 1996

Microsatellite instability in early onset and familial colorectal cancerC Brassett, J A Joyce, N J Froggatt, et al.

Journal of Medical Genetics|April 25, 2000

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndromeD Catchpoole, A V Smallwood, J A Joyce, et al.

Oncogene|May 7, 2013

Heparanase promotes lymphangiogenesis and tumor invasion in pancreatic neuroendocrine tumorsK E Hunter, C Palermo, J C Kester, et al.

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.

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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