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M C King

Showing results (171-180 of 186) with videos related to

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Computers and Biomedical Research, an International Journal|June 1, 1994
An automated technique for identification and analysis of activation fronts in a two-dimensional electrogram arrayK D Bollacker, E V Simpson, R E Hillsley, et al.
Tissue Antigens|February 16, 2000
Hardy-Weinberg testing for HLA class II (DRB1, DQA1, DQB1, and DPB1) loci in 26 human ethnic groupsJ J Chen, J A Hollenbach, E A Trachtenberg, et al.
American Journal of Human Genetics|December 18, 1997
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposisE D Lynch, E A Ostermeyer, M K Lee, et al.
Progress in Clinical and Biological Research|January 1, 1977
HLA in breast cancer-prone families and the cancer family syndromeH T Lynch, P I Terasaki, H A Guirgis, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
British Journal of Cancer|February 22, 2000
Evidence of a founder BRCA1 mutation in ScotlandA Liede, B Cohen, D M Black, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
Genomics|October 15, 1996
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1K J Abel, L C Brody, J M Valdes, et al.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
The British Journal of Dermatology|April 12, 2019
Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patientsE Chasseuil, J A McGrath, A Seo, et al.
Pageof 19

Showing results (171-180 of 186) with videos related to

Sort By:
Pageof 19
Computers and Biomedical Research, an International Journal|June 1, 1994
An automated technique for identification and analysis of activation fronts in a two-dimensional electrogram arrayK D Bollacker, E V Simpson, R E Hillsley, et al.
Tissue Antigens|February 16, 2000
Hardy-Weinberg testing for HLA class II (DRB1, DQA1, DQB1, and DPB1) loci in 26 human ethnic groupsJ J Chen, J A Hollenbach, E A Trachtenberg, et al.
American Journal of Human Genetics|December 18, 1997
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposisE D Lynch, E A Ostermeyer, M K Lee, et al.
Progress in Clinical and Biological Research|January 1, 1977
HLA in breast cancer-prone families and the cancer family syndromeH T Lynch, P I Terasaki, H A Guirgis, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
British Journal of Cancer|February 22, 2000
Evidence of a founder BRCA1 mutation in ScotlandA Liede, B Cohen, D M Black, et al.
Clinical Genetics|May 9, 2014
Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X)M J Basehore, R Michaelson-Cohen, E Levy-Lahad, et al.
Genomics|October 15, 1996
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1K J Abel, L C Brody, J M Valdes, et al.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
The British Journal of Dermatology|April 12, 2019
Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patientsE Chasseuil, J A McGrath, A Seo, et al.
Pageof 19