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M C King

Showing results (181-190 of 186) with videos related to

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Familial Cancer|April 10, 2021
A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancerI Kedar, L Walsh, G Reznick Levi, et al.
American Journal of Human Genetics|February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyS L Neuhausen, S Mazoyer, L Friedman, et al.
Nature Genetics|September 10, 1998
The APCI1307K allele and breast cancer riskM Redston, K L Nathanson, Z Q Yuan, et al.
Science (New York, N.Y.)|February 1, 2020
Genetics of schizophrenia in the South African XhosaS Gulsuner, D J Stein, E S Susser, et al.
American Journal of Human Genetics|June 19, 1998
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international studyS L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
American Journal of Human Genetics|November 28, 2002
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish populationW D Foulkes, I Thiffault, S B Gruber, et al.
Pageof 19

Showing results (181-190 of 186) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 186 results.
Familial Cancer|April 10, 2021
A novel founder MSH2 deletion in Ethiopian Jews is mainly associated with early-onset colorectal cancerI Kedar, L Walsh, G Reznick Levi, et al.
American Journal of Human Genetics|February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international studyS L Neuhausen, S Mazoyer, L Friedman, et al.
Nature Genetics|September 10, 1998
The APCI1307K allele and breast cancer riskM Redston, K L Nathanson, Z Q Yuan, et al.
Science (New York, N.Y.)|February 1, 2020
Genetics of schizophrenia in the South African XhosaS Gulsuner, D J Stein, E S Susser, et al.
American Journal of Human Genetics|June 19, 1998
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international studyS L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
American Journal of Human Genetics|November 28, 2002
The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish populationW D Foulkes, I Thiffault, S B Gruber, et al.
Pageof 19