Search research articles
Contact Us
Filters
Showing results (11-20 of 45) with videos related to
Page
of 5
Sort By:
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1973
Regional localization of loci for human PGM and 6PGD on human chromosome one by use of hybrids of Chinese hamster-human somatic cells
G R Douglas, P J McAlpine, J L Hamerton
Biochemical Genetics
|
June 1, 1980
Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter leads to q21
L J Donald, H S Wang, J L Hamerton
Genomics
|
March 1, 1991
Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR)
A J Kirkilionis, C A Gregory, J L Hamerton
American Journal of Human Genetics
|
August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
C R Greenberg, J L Hamerton, M Nigli, et al.
Pediatric Research
|
September 1, 1978
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease
S D Pena, N M Quilliam, J L Hamerton, et al.
Journal of Medical Genetics
|
March 1, 1975
Deletion of the short arm of chromosome No. 10
M H Shokeir, M Ray, J L Hamerton, et al.
Somatic Cell and Molecular Genetics
|
May 1, 1989
The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7
Y Myal, C Gregory, H Wang, et al.
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie
|
January 1, 1981
The effects of gamma irradiation of human fibroblasts on human/Chinese hamster somatic cell hybrids
L J Donald, H S Wang, N J Holliday, et al.
Clinical Genetics
|
July 1, 1978
Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy
S D Pena, A Vust, D Tucker, et al.
Canadian Medical Association Journal
|
April 8, 1972
Chromosome studies in a neonatal population
J L Hamerton, M Ray, J Abbott, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1973
Regional localization of loci for human PGM and 6PGD on human chromosome one by use of hybrids of Chinese hamster-human somatic cells
G R Douglas, P J McAlpine, J L Hamerton
Biochemical Genetics
|
June 1, 1980
Assignment of the sorbitol dehydrogenase locus to human chromosome 15 pter leads to q21
L J Donald, H S Wang, J L Hamerton
Genomics
|
March 1, 1991
Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR)
A J Kirkilionis, C A Gregory, J L Hamerton
American Journal of Human Genetics
|
August 1, 1987
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21
C R Greenberg, J L Hamerton, M Nigli, et al.
Pediatric Research
|
September 1, 1978
Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease
S D Pena, N M Quilliam, J L Hamerton, et al.
Journal of Medical Genetics
|
March 1, 1975
Deletion of the short arm of chromosome No. 10
M H Shokeir, M Ray, J L Hamerton, et al.
Somatic Cell and Molecular Genetics
|
May 1, 1989
The gene for prolactin-inducible protein (PIP), uniquely expressed in exocrine organs, maps to chromosome 7
Y Myal, C Gregory, H Wang, et al.
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie
|
January 1, 1981
The effects of gamma irradiation of human fibroblasts on human/Chinese hamster somatic cell hybrids
L J Donald, H S Wang, N J Holliday, et al.
Clinical Genetics
|
July 1, 1978
Biochemical investigations in cultured skin fibroblasts from patients with Duchenne muscular dystrophy
S D Pena, A Vust, D Tucker, et al.
Canadian Medical Association Journal
|
April 8, 1972
Chromosome studies in a neonatal population
J L Hamerton, M Ray, J Abbott, et al.
Page
of 5