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Human Molecular Genetics
|
June 1, 1995
Distribution of 13 truncating mutations in the neurofibromatosis 1 gene
R 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 infection
C 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 status
C 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 fibrosis
W E Highsmith, L H Burch, Z Zhou, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 84) with videos related to
Sort By:
Page
of 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 gene
R 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 infection
C 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 status
C 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 fibrosis
W E Highsmith, L H Burch, Z Zhou, et al.
Page
of 9