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Birth Defects Original Article Series
|
January 11, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysis
M W Thompson, C T Falk, R G Worton, et al.
Cytogenetics and Cell Genetics
|
January 1, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysis
M W Thompson, C T Falk, R G Worton, et al.
American Journal of Human Genetics
|
September 1, 1974
Linkage studies in a large kindred with familial hypercholesterolemia
J Ott, H G Schrott, J L Goldstein, et al.
Neuron
|
May 1, 1989
Human gene for torsion dystonia located on chromosome 9q32-q34
L Ozelius, P L Kramer, C B Moskowitz, et al.
Human Genetics
|
January 1, 1984
Estimating the recombination frequency for the PTC-Kell linkage
M Anne-Spence, C T Falk, K Neiswanger, et al.
American Journal of Human Genetics
|
November 15, 2000
Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1
D M Reynolds, C T Falk, A Li, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
Birth Defects Original Article Series
|
January 11, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysis
M W Thompson, C T Falk, R G Worton, et al.
Cytogenetics and Cell Genetics
|
January 1, 1976
A report on a family with a (1;2) translocation: cytologic and linkage analysis
M W Thompson, C T Falk, R G Worton, et al.
American Journal of Human Genetics
|
September 1, 1974
Linkage studies in a large kindred with familial hypercholesterolemia
J Ott, H G Schrott, J L Goldstein, et al.
Neuron
|
May 1, 1989
Human gene for torsion dystonia located on chromosome 9q32-q34
L Ozelius, P L Kramer, C B Moskowitz, et al.
Human Genetics
|
January 1, 1984
Estimating the recombination frequency for the PTC-Kell linkage
M Anne-Spence, C T Falk, K Neiswanger, et al.
American Journal of Human Genetics
|
November 15, 2000
Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1
D M Reynolds, C T Falk, A Li, et al.
Page
of 5