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M C King

Showing results (121-130 of 186) with videos related to

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Breast Disease|February 3, 2005
Gene therapy for breast and ovarian cancer with BRCA1D L Tait, R A Jensen, J T Holt, et al.
American Journal of Public Health|June 1, 1990
Nongenetic influences of obesity on other cardiovascular disease risk factors: an analysis of identical twinsB Newman, J V Selby, C P Quesenberry, et al.
Genomics|September 1, 1993
High-density genetic map of the BRCA1 region of chromosome 17q12-q21L A Anderson, L Friedman, S Osborne-Lawrence, et al.
Clinical Genetics|February 26, 2011
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing lossK O Yariz, T Walsh, H Akay, et al.
Genetic Testing|January 1, 1997
BRCA1 and BRCA2 mutations in Ashkenazi Jewish families with breast and ovarian cancerE L Schubert, H C Mefford, J L Dann, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 1, 1977
Gynecologic specimen adequacy for flow system experimentsE B King, D L Barrett, E C Hill, et al.
Genomics|October 1, 1991
Call for a worldwide survey of human genetic diversity: a vanishing opportunity for the Human Genome ProjectL L Cavalli-Sforza, A C Wilson, C R Cantor, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1980
Diagnosis of twin zygosity by self-assessment and by genetic analysisM C King, G D Friedman, D Lattanzio, et al.
The Journal of School Health|May 1, 1995
A statewide institute to deliver professional development programs to school health personnel in MassachusettsP W Piessens, M C King, J Ryan, et al.
Science (New York, N.Y.)|November 21, 1997
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanousE D Lynch, M K Lee, J E Morrow, et al.
Pageof 19

Showing results (121-130 of 186) with videos related to

Sort By:
Pageof 19
Breast Disease|February 3, 2005
Gene therapy for breast and ovarian cancer with BRCA1D L Tait, R A Jensen, J T Holt, et al.
American Journal of Public Health|June 1, 1990
Nongenetic influences of obesity on other cardiovascular disease risk factors: an analysis of identical twinsB Newman, J V Selby, C P Quesenberry, et al.
Genomics|September 1, 1993
High-density genetic map of the BRCA1 region of chromosome 17q12-q21L A Anderson, L Friedman, S Osborne-Lawrence, et al.
Clinical Genetics|February 26, 2011
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing lossK O Yariz, T Walsh, H Akay, et al.
Genetic Testing|January 1, 1997
BRCA1 and BRCA2 mutations in Ashkenazi Jewish families with breast and ovarian cancerE L Schubert, H C Mefford, J L Dann, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|July 1, 1977
Gynecologic specimen adequacy for flow system experimentsE B King, D L Barrett, E C Hill, et al.
Genomics|October 1, 1991
Call for a worldwide survey of human genetic diversity: a vanishing opportunity for the Human Genome ProjectL L Cavalli-Sforza, A C Wilson, C R Cantor, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1980
Diagnosis of twin zygosity by self-assessment and by genetic analysisM C King, G D Friedman, D Lattanzio, et al.
The Journal of School Health|May 1, 1995
A statewide institute to deliver professional development programs to school health personnel in MassachusettsP W Piessens, M C King, J Ryan, et al.
Science (New York, N.Y.)|November 21, 1997
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanousE D Lynch, M K Lee, J E Morrow, et al.
Pageof 19