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H Asher

Showing results (11-20 of 46) with videos related to

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Journal of Medical Genetics|October 1, 1990
Mouse and hamster mutants as models for Waardenburg syndromes in humansJ H Asher, T B Friedman
The Journal of Experimental Zoology|December 1, 1981
A histological examination of the pars distalis from the Syrian hamster mutant Anophthalmic white (Wh)S C James, J H Asher
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1982
The primary ultrastructural defect caused by anophthalmic white (Wh) in the Syrian hamsterJ H Asher, S C James
Annals of the New York Academy of Sciences|January 1, 1991
Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPPJ H Asher, R Morell, T B Friedman
Human Molecular Genetics|September 1, 1993
A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) familyR Morell, T B Friedman, J H Asher
The Journal of Experimental Zoology|December 1, 1980
Effects of the gene Wh on reproduction in the Syrian hamster, Mesocricetus auratusS C James, G Hooper, J H Asher
American Journal of Human Genetics|January 11, 1991
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2qJ H Asher, R Morell, T B Friedman
Genetics|October 1, 1970
Parthenogenesis and genetic variability. I. Linkage and inbreeding estimations in the frog, Rana pipiensG W Nace, C M Richards, J H Asher
The Journal of Heredity|September 1, 1974
A new mutant in the yellow-bellied cotton ratD W McWhirter, P L Dalby, J H Asher
Human Mutation|January 1, 1996
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndromeJ H Asher, A Sommer, R Morell, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|October 1, 1990
Mouse and hamster mutants as models for Waardenburg syndromes in humansJ H Asher, T B Friedman
The Journal of Experimental Zoology|December 1, 1981
A histological examination of the pars distalis from the Syrian hamster mutant Anophthalmic white (Wh)S C James, J H Asher
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1982
The primary ultrastructural defect caused by anophthalmic white (Wh) in the Syrian hamsterJ H Asher, S C James
Annals of the New York Academy of Sciences|January 1, 1991
Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPPJ H Asher, R Morell, T B Friedman
Human Molecular Genetics|September 1, 1993
A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) familyR Morell, T B Friedman, J H Asher
The Journal of Experimental Zoology|December 1, 1980
Effects of the gene Wh on reproduction in the Syrian hamster, Mesocricetus auratusS C James, G Hooper, J H Asher
American Journal of Human Genetics|January 11, 1991
Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2qJ H Asher, R Morell, T B Friedman
Genetics|October 1, 1970
Parthenogenesis and genetic variability. I. Linkage and inbreeding estimations in the frog, Rana pipiensG W Nace, C M Richards, J H Asher
The Journal of Heredity|September 1, 1974
A new mutant in the yellow-bellied cotton ratD W McWhirter, P L Dalby, J H Asher
Human Mutation|January 1, 1996
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndromeJ H Asher, A Sommer, R Morell, et al.
Pageof 5