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Nazneen Rahman

Showing results (71-80 of 154) with videos related to

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American Journal of Human Genetics|May 6, 2017
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual DisabilityKatrina Tatton-Brown, Chey Loveday, Shawn Yost, et al.
Nature Genetics|October 13, 2006
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility allelesSheila Seal, Deborah Thompson, Anthony Renwick, et al.
Nature Genetics|January 4, 2007
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility geneNazneen Rahman, Sheila Seal, Deborah Thompson, et al.
Nature Communications|August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumourSandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Human Molecular Genetics|June 20, 2014
Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumorsRoelof Koster, Nandita Mitra, Kurt D'Andrea, et al.
International Journal of Cancer|December 31, 2005
Evaluation of RAD50 in familial breast cancer predispositionJohanna Tommiska, Sheila Seal, Anthony Renwick, et al.
American Journal of Human Genetics|September 6, 2002
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.
Nature Genetics|June 2, 2009
A genome-wide association study of testicular germ cell tumorElizabeth A Rapley, Clare Turnbull, Ali Amin Al Olama, et al.
American Journal of Human Genetics|May 31, 2003
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.
Nature Genetics|April 20, 2010
Mutation of the RAD51C gene in a Fanconi anemia-like disorderFiona Vaz, Helmut Hanenberg, Beatrice Schuster, et al.
Pageof 16

Showing results (71-80 of 154) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|May 6, 2017
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual DisabilityKatrina Tatton-Brown, Chey Loveday, Shawn Yost, et al.
Nature Genetics|October 13, 2006
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility allelesSheila Seal, Deborah Thompson, Anthony Renwick, et al.
Nature Genetics|January 4, 2007
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility geneNazneen Rahman, Sheila Seal, Deborah Thompson, et al.
Nature Communications|August 8, 2014
Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumourSandra Hanks, Elizabeth R Perdeaux, Sheila Seal, et al.
Human Molecular Genetics|June 20, 2014
Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumorsRoelof Koster, Nandita Mitra, Kurt D'Andrea, et al.
International Journal of Cancer|December 31, 2005
Evaluation of RAD50 in familial breast cancer predispositionJohanna Tommiska, Sheila Seal, Anthony Renwick, et al.
American Journal of Human Genetics|September 6, 2002
The gene for juvenile hyaline fibromatosis maps to chromosome 4q21Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.
Nature Genetics|June 2, 2009
A genome-wide association study of testicular germ cell tumorElizabeth A Rapley, Clare Turnbull, Ali Amin Al Olama, et al.
American Journal of Human Genetics|May 31, 2003
Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13Nazneen Rahman, Melanie Dunstan, M Dawn Teare, et al.
Nature Genetics|April 20, 2010
Mutation of the RAD51C gene in a Fanconi anemia-like disorderFiona Vaz, Helmut Hanenberg, Beatrice Schuster, et al.
Pageof 16