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Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1995
The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouseD A Adler, N A Quaderi, S D Brown, et al.
Genomics|November 1, 1988
Molecular and genetic mapping of the mouse mdx locusJ S Cavanna, G Coulton, J E Morgan, et al.
Nature Genetics|June 1, 1997
Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessX Z Liu, J Walsh, P Mburu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 22, 1999
A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidateA J Paige, B W Kiernan, A Varela, et al.
Genomics|February 1, 1992
Rps4 maps near the inactivation center on the mouse X chromosomeR M Hamvas, A Zinn, J T Keer, et al.
Journal of Clinical Microbiology|June 1, 1985
Ciprofloxacin disk susceptibility tests: interpretive zone size standards for 5-microgram disksA L Barry, R J Fass, J P Anhalt, et al.
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