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Molecular Psychiatry|March 8, 2017

Risk alleles of genes with monoallelic expression are enriched in gain-of-function variants and depleted in loss-of-function variants for neurodevelopmental disordersV Savova, S Vinogradova, D Pruss, et al.

Journal of Human Genetics|February 24, 2001

The BRCA2 genetic variant IVS7 + 2T-->G is a mutationM T Pyne, A R Brothman, B Ward, et al.

Nucleic Acids Research|May 24, 1985

Primary organization of nucleosomal core particles is invariable in repressed and active nuclei from animal, plant and yeast cellsS G Bavykin, S I Usachenko, A I Lishanskaya, et al.

Science (New York, N.Y.)|October 25, 1996

An asymmetric model for the nucleosome: a binding site for linker histones inside the DNA gyresD Pruss, B Bartholomew, J Persinger, et al.

Clinical Genetics|February 3, 2015

Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genesE T Rosenthal, K R Bowles, D Pruss, et al.

Clinical Genetics|December 6, 2013

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genesJ M Eggington, K R Bowles, K Moyes, et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 20, 2018

Breast cancer brain metastases show increased levels of genomic aberration-based homologous recombination deficiency scores relative to their corresponding primary tumorsM Diossy, L Reiniger, Z Sztupinszki, et al.

JAMA|October 23, 1997

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testingD Shattuck-Eidens, A Oliphant, M McClure, et al.

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Showing results (31-40 of 38) with videos related to

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You have reached the last page of results.This site can display upto 38 results.

Molecular Psychiatry|March 8, 2017

Risk alleles of genes with monoallelic expression are enriched in gain-of-function variants and depleted in loss-of-function variants for neurodevelopmental disordersV Savova, S Vinogradova, D Pruss, et al.

Journal of Human Genetics|February 24, 2001

The BRCA2 genetic variant IVS7 + 2T-->G is a mutationM T Pyne, A R Brothman, B Ward, et al.

Nucleic Acids Research|May 24, 1985

Primary organization of nucleosomal core particles is invariable in repressed and active nuclei from animal, plant and yeast cellsS G Bavykin, S I Usachenko, A I Lishanskaya, et al.

Science (New York, N.Y.)|October 25, 1996

An asymmetric model for the nucleosome: a binding site for linker histones inside the DNA gyresD Pruss, B Bartholomew, J Persinger, et al.

Clinical Genetics|February 3, 2015

Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genesE T Rosenthal, K R Bowles, D Pruss, et al.

Clinical Genetics|December 6, 2013

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genesJ M Eggington, K R Bowles, K Moyes, et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 20, 2018

Breast cancer brain metastases show increased levels of genomic aberration-based homologous recombination deficiency scores relative to their corresponding primary tumorsM Diossy, L Reiniger, Z Sztupinszki, et al.

JAMA|October 23, 1997

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testingD Shattuck-Eidens, A Oliphant, M McClure, et al.

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