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Nazneen Rahman

Showing results (61-70 of 154) with videos related to

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Nature Genetics|October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1BSandra Hanks, Kim Coleman, Sarah Reid, et al.
JAMA Network Open|May 25, 2019
Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast CancerZoe Kemp, Alice Turnbull, Shawn Yost, et al.
Kidney International|October 9, 2003
Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domainsMatthias T F Wolf, Bettina E Mucha, Massimo Attanasio, et al.
Cancer Research|September 6, 2005
Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridizationGöran Jönsson, Tara L Naylor, Johan Vallon-Christersson, et al.
Plos Genetics|May 26, 2017
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastomaLee D McDaniel, Karina L Conkrite, Xiao Chang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 21, 2007
Estrogen receptor status could modulate the genomic pattern in familial and sporadic breast cancerLorenzo Melchor, Emiliano Honrado, Jia Huang, et al.
Nature Genetics|July 17, 2007
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowthJenny Douglas, Deirdre Cilliers, Kim Coleman, et al.
Nature Genetics|July 13, 2006
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility allelesAnthony Renwick, Deborah Thompson, Sheila Seal, et al.
Nature Genetics|June 15, 2010
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancerClare Turnbull, Elizabeth A Rapley, Sheila Seal, et al.
American Journal of Human Genetics|June 9, 2005
Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrationsKatrina Tatton-Brown, Jenny Douglas, Kim Coleman, et al.
Pageof 16

Showing results (61-70 of 154) with videos related to

Sort By:
Pageof 16
Nature Genetics|October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1BSandra Hanks, Kim Coleman, Sarah Reid, et al.
JAMA Network Open|May 25, 2019
Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast CancerZoe Kemp, Alice Turnbull, Shawn Yost, et al.
Kidney International|October 9, 2003
Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domainsMatthias T F Wolf, Bettina E Mucha, Massimo Attanasio, et al.
Cancer Research|September 6, 2005
Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridizationGöran Jönsson, Tara L Naylor, Johan Vallon-Christersson, et al.
Plos Genetics|May 26, 2017
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastomaLee D McDaniel, Karina L Conkrite, Xiao Chang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 21, 2007
Estrogen receptor status could modulate the genomic pattern in familial and sporadic breast cancerLorenzo Melchor, Emiliano Honrado, Jia Huang, et al.
Nature Genetics|July 17, 2007
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowthJenny Douglas, Deirdre Cilliers, Kim Coleman, et al.
Nature Genetics|July 13, 2006
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility allelesAnthony Renwick, Deborah Thompson, Sheila Seal, et al.
Nature Genetics|June 15, 2010
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancerClare Turnbull, Elizabeth A Rapley, Sheila Seal, et al.
American Journal of Human Genetics|June 9, 2005
Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrationsKatrina Tatton-Brown, Jenny Douglas, Kim Coleman, et al.
Pageof 16