Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nazneen Rahman

Showing results (81-90 of 154) with videos related to

Pageof 16
Sort By:
American Journal of Human Genetics|March 1, 2003
Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibilityMieke Schutte, Sheila Seal, Rita Barfoot, et al.
American Journal of Medical Genetics. Part A|January 13, 2009
15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15qKatrina Tatton-Brown, Daniela T Pilz, Karen Helene Orstavik, et al.
Nature Genetics|January 4, 2007
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancerSarah Reid, Detlev Schindler, Helmut Hanenberg, et al.
Nature Genetics|May 14, 2013
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14Elise Ruark, Sheila Seal, Heather McDonald, et al.
Human Molecular Genetics|October 5, 2014
Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25Kevin Litchfield, Razvan Sultana, Anthony Renwick, et al.
Nature Genetics|May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregationShawn Yost, Bas de Wolf, Sandra Hanks, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 14, 2006
A multicenter study of cancer incidence in CHEK2 1100delC mutation carriersDeborah Thompson, Sheila Seal, Mieke Schutte, et al.
Nature Genetics|May 10, 2011
Mutations in CEP57 cause mosaic variegated aneuploidy syndromeKatie Snape, Sandra Hanks, Elise Ruark, et al.
American Journal of Human Genetics|September 26, 2003
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosisSandra Hanks, Sarah Adams, Jenny Douglas, et al.
Nature Genetics|October 7, 2008
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumorRichard H Scott, Jenny Douglas, Linda Baskcomb, et al.
Pageof 16

Showing results (81-90 of 154) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|March 1, 2003
Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibilityMieke Schutte, Sheila Seal, Rita Barfoot, et al.
American Journal of Medical Genetics. Part A|January 13, 2009
15q overgrowth syndrome: a newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15qKatrina Tatton-Brown, Daniela T Pilz, Karen Helene Orstavik, et al.
Nature Genetics|January 4, 2007
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancerSarah Reid, Detlev Schindler, Helmut Hanenberg, et al.
Nature Genetics|May 14, 2013
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14Elise Ruark, Sheila Seal, Heather McDonald, et al.
Human Molecular Genetics|October 5, 2014
Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25Kevin Litchfield, Razvan Sultana, Anthony Renwick, et al.
Nature Genetics|May 30, 2017
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregationShawn Yost, Bas de Wolf, Sandra Hanks, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 14, 2006
A multicenter study of cancer incidence in CHEK2 1100delC mutation carriersDeborah Thompson, Sheila Seal, Mieke Schutte, et al.
Nature Genetics|May 10, 2011
Mutations in CEP57 cause mosaic variegated aneuploidy syndromeKatie Snape, Sandra Hanks, Elise Ruark, et al.
American Journal of Human Genetics|September 26, 2003
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosisSandra Hanks, Sarah Adams, Jenny Douglas, et al.
Nature Genetics|October 7, 2008
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumorRichard H Scott, Jenny Douglas, Linda Baskcomb, et al.
Pageof 16