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Genomics
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November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium
B J Keats, A A Todorov, L D Atwood, et al.
American Journal of Medical Genetics
|
March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium
R J Smith, C I Berlin, J F Hejtmancik, et al.
Nature Genetics
|
September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
E Verpy, M Leibovici, I Zwaenepoel, et al.
American Journal of Human Genetics
|
October 1, 1987
Linkage studies of Friedreich ataxia by means of blood-group and protein markers
B J Keats, L J Ward, M Lu, et al.
Genomics
|
December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11
R J Smith, E C Lee, W J Kimberling, et al.
Genomics
|
March 1, 1991
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990)
B J Keats, S L Sherman, N E Morton, et al.
Annals of Human Genetics
|
January 1, 1991
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990)
B J Keats, S L Sherman, N E Morton, et al.
Nature Genetics
|
June 1, 1994
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10
R A Preston, J C Post, B J Keats, et al.
Leukemia
|
February 13, 2014
Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myeloma
Maurizio Affer, Marta Chesi, Wei-Dong G Chen, et al.
Blood
|
February 4, 2011
RNAi screen of the druggable genome identifies modulators of proteasome inhibitor sensitivity in myeloma including CDK5
Yuan Xiao Zhu, Rodger Tiedemann, Chang-Xin Shi, et al.
Page
of 15
Search research articles
Search
Showing results (81-90 of 149) with videos related to
Sort By:
Page
of 15
Genomics
|
November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium
B J Keats, A A Todorov, L D Atwood, et al.
American Journal of Medical Genetics
|
March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium
R J Smith, C I Berlin, J F Hejtmancik, et al.
Nature Genetics
|
September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
E Verpy, M Leibovici, I Zwaenepoel, et al.
American Journal of Human Genetics
|
October 1, 1987
Linkage studies of Friedreich ataxia by means of blood-group and protein markers
B J Keats, L J Ward, M Lu, et al.
Genomics
|
December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11
R J Smith, E C Lee, W J Kimberling, et al.
Genomics
|
March 1, 1991
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990)
B J Keats, S L Sherman, N E Morton, et al.
Annals of Human Genetics
|
January 1, 1991
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990)
B J Keats, S L Sherman, N E Morton, et al.
Nature Genetics
|
June 1, 1994
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10
R A Preston, J C Post, B J Keats, et al.
Leukemia
|
February 13, 2014
Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myeloma
Maurizio Affer, Marta Chesi, Wei-Dong G Chen, et al.
Blood
|
February 4, 2011
RNAi screen of the druggable genome identifies modulators of proteasome inhibitor sensitivity in myeloma including CDK5
Yuan Xiao Zhu, Rodger Tiedemann, Chang-Xin Shi, et al.
Page
of 15