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David Goldgar

Showing results (11-20 of 75) with videos related to

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Journal of Cutaneous Pathology|May 25, 2010
Anatomic variability in superficial blood vessel and lymphatic vessel densityKeith Duffy, Mark A Hyde, Brad Tanner, et al.
Human Molecular Genetics|May 23, 2002
CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5qKatherine L Nathanson, Yin Y Shugart, Romaica Omaruddin, et al.
Human Mutation|January 4, 2020
Differences in patient ascertainment affect the use of gene-specified ACMG/AMP phenotype-related variant classification criteria: Evidence for TP53Cristina Fortuno, Tina Pesaran, Jill Dolinsky, et al.
Genes, Chromosomes & Cancer|December 16, 2006
The M53I mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestryJulie Lang, Nicholas Hayward, David Goldgar, et al.
Cancer Research|February 8, 2005
Functional evaluation and cancer risk assessment of BRCA2 unclassified variantsKangjian Wu, Shannon R Hinson, Akihiro Ohashi, et al.
Human Mutation|July 17, 2021
An updated quantitative model to classify missense variants in the TP53 gene: A novel multifactorial strategyCristina Fortuno, Tina Pesaran, Jill Dolinsky, et al.
International Journal of Cancer|December 3, 2003
Role of CHEK2*1100delC in unselected series of non-BRCA1/2 male breast cancersSusan Neuhausen, Alison Dunning, Linda Steele, et al.
Journal of Dermatological Science|October 30, 2012
Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigreeJason E Hawkes, Pamela B Cassidy, Prashiela Manga, et al.
The Breast Journal|June 27, 2013
Can unknown predisposition in familial breast cancer be family-specific?Henry Lynch, Hongxiu Wen, Yeong C Kim, et al.
Human Mutation|November 21, 2002
BRCA1 and BRCA2 sequence variants in Chinese breast cancer familiesXiangcheng Zhi, Csilla Szabo, Sandrine Chopin, et al.
Pageof 8

Showing results (11-20 of 75) with videos related to

Sort By:
Pageof 8
Journal of Cutaneous Pathology|May 25, 2010
Anatomic variability in superficial blood vessel and lymphatic vessel densityKeith Duffy, Mark A Hyde, Brad Tanner, et al.
Human Molecular Genetics|May 23, 2002
CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5qKatherine L Nathanson, Yin Y Shugart, Romaica Omaruddin, et al.
Human Mutation|January 4, 2020
Differences in patient ascertainment affect the use of gene-specified ACMG/AMP phenotype-related variant classification criteria: Evidence for TP53Cristina Fortuno, Tina Pesaran, Jill Dolinsky, et al.
Genes, Chromosomes & Cancer|December 16, 2006
The M53I mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestryJulie Lang, Nicholas Hayward, David Goldgar, et al.
Cancer Research|February 8, 2005
Functional evaluation and cancer risk assessment of BRCA2 unclassified variantsKangjian Wu, Shannon R Hinson, Akihiro Ohashi, et al.
Human Mutation|July 17, 2021
An updated quantitative model to classify missense variants in the TP53 gene: A novel multifactorial strategyCristina Fortuno, Tina Pesaran, Jill Dolinsky, et al.
International Journal of Cancer|December 3, 2003
Role of CHEK2*1100delC in unselected series of non-BRCA1/2 male breast cancersSusan Neuhausen, Alison Dunning, Linda Steele, et al.
Journal of Dermatological Science|October 30, 2012
Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigreeJason E Hawkes, Pamela B Cassidy, Prashiela Manga, et al.
The Breast Journal|June 27, 2013
Can unknown predisposition in familial breast cancer be family-specific?Henry Lynch, Hongxiu Wen, Yeong C Kim, et al.
Human Mutation|November 21, 2002
BRCA1 and BRCA2 sequence variants in Chinese breast cancer familiesXiangcheng Zhi, Csilla Szabo, Sandrine Chopin, et al.
Pageof 8