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Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant
J A Trofatter, S R Dlouhy, W DeMyer, et al.
American Journal of Human Genetics
|
July 1, 1970
Genetic linkage analysis of human hemoglobin variants
W E Nance, M Conneally, K W Kang, et al.
American Journal of Medical Genetics
|
January 1, 1988
Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28
M Kambouris, S R Dlouhy, J A Trofatter, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Genetic analysis of urinary pepsinogen isozymes
R T Taggart, P L Yu, R C Karn, et al.
American Journal of Medical Genetics
|
May 1, 1984
Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome)
M G Butler, M E Hodes, P M Conneally, et al.
The Journal of Clinical Investigation
|
January 1, 1988
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis
M R Wallace, F E Dwulet, E C Williams, et al.
Human Genetics
|
November 1, 1979
Urinary pepsinogen isozymes: a highly polymorphic locus in man
R T Taggart, R C Karn, A D Merritt, et al.
Human Genetics
|
February 1, 1987
Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter
S R Dlouhy, J C Christian, J L Haines, et al.
Journal of Medical Genetics
|
April 1, 1993
Suicide risk in Huntington's disease
L Di Maio, F Squitieri, G Napolitano, et al.
American Journal of Human Genetics
|
July 1, 1980
Linkage relationships and multipoint mapping of the human parotid salivary proteins (Pr, Pa, Db)
P L Yu, R C Karn, A D Merritt, et al.
Page
of 20
Search research articles
Search
Showing results (71-80 of 194) with videos related to
Sort By:
Page
of 20
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant
J A Trofatter, S R Dlouhy, W DeMyer, et al.
American Journal of Human Genetics
|
July 1, 1970
Genetic linkage analysis of human hemoglobin variants
W E Nance, M Conneally, K W Kang, et al.
American Journal of Medical Genetics
|
January 1, 1988
Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28
M Kambouris, S R Dlouhy, J A Trofatter, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Genetic analysis of urinary pepsinogen isozymes
R T Taggart, P L Yu, R C Karn, et al.
American Journal of Medical Genetics
|
May 1, 1984
Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome)
M G Butler, M E Hodes, P M Conneally, et al.
The Journal of Clinical Investigation
|
January 1, 1988
Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis
M R Wallace, F E Dwulet, E C Williams, et al.
Human Genetics
|
November 1, 1979
Urinary pepsinogen isozymes: a highly polymorphic locus in man
R T Taggart, R C Karn, A D Merritt, et al.
Human Genetics
|
February 1, 1987
Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter
S R Dlouhy, J C Christian, J L Haines, et al.
Journal of Medical Genetics
|
April 1, 1993
Suicide risk in Huntington's disease
L Di Maio, F Squitieri, G Napolitano, et al.
American Journal of Human Genetics
|
July 1, 1980
Linkage relationships and multipoint mapping of the human parotid salivary proteins (Pr, Pa, Db)
P L Yu, R C Karn, A D Merritt, et al.
Page
of 20