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Nature Genetics
|
October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
Sandra 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 Cancer
Zoe 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 domains
Matthias 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 hybridization
Göran 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 neuroblastoma
Lee 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 cancer
Lorenzo 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 overgrowth
Jenny Douglas, Deirdre Cilliers, Kim Coleman, et al.
Nature Genetics
|
July 13, 2006
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
Anthony Renwick, Deborah Thompson, Sheila Seal, et al.
Nature Genetics
|
June 15, 2010
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer
Clare 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 aberrations
Katrina Tatton-Brown, Jenny Douglas, Kim Coleman, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 154) with videos related to
Sort By:
Page
of 16
Nature Genetics
|
October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
Sandra 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 Cancer
Zoe 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 domains
Matthias 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 hybridization
Göran 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 neuroblastoma
Lee 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 cancer
Lorenzo 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 overgrowth
Jenny Douglas, Deirdre Cilliers, Kim Coleman, et al.
Nature Genetics
|
July 13, 2006
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
Anthony Renwick, Deborah Thompson, Sheila Seal, et al.
Nature Genetics
|
June 15, 2010
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer
Clare 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 aberrations
Katrina Tatton-Brown, Jenny Douglas, Kim Coleman, et al.
Page
of 16