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L M Silverman

Showing results (81-90 of 84) with videos related to

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Human Molecular Genetics|June 1, 1995
Distribution of 13 truncating mutations in the neurofibromatosis 1 geneR A Heim, L N Kam-Morgan, C G Binnie, et al.
Annals of Clinical and Laboratory Science|May 1, 1992
Cerebrospinal fluid analysis in human immunodeficiency virus infectionC D Hall, C R Snyder, K R Robertson, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1992
Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier statusC A Quigley, K J Friedman, A Johnson, et al.
Human Mutation|January 1, 1997
Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosisW E Highsmith, L H Burch, Z Zhou, et al.
Pageof 9

Showing results (81-90 of 84) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 84 results.
Human Molecular Genetics|June 1, 1995
Distribution of 13 truncating mutations in the neurofibromatosis 1 geneR A Heim, L N Kam-Morgan, C G Binnie, et al.
Annals of Clinical and Laboratory Science|May 1, 1992
Cerebrospinal fluid analysis in human immunodeficiency virus infectionC D Hall, C R Snyder, K R Robertson, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1992
Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier statusC A Quigley, K J Friedman, A Johnson, et al.
Human Mutation|January 1, 1997
Identification of a splice site mutation (2789 +5 G > A) associated with small amounts of normal CFTR mRNA and mild cystic fibrosisW E Highsmith, L H Burch, Z Zhou, et al.
Pageof 9