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Nucleic Acids Research
|
February 25, 1988
A fragment of the human c-Ki-ras1 pseudogene (HGM9 gene symbol KRAS1P), localized to 6p12-p11, detects 3 allele, RFLP
H Blanché, E H Chang, J Dausset, et al.
Cytogenetics and Cell Genetics
|
January 1, 1996
Detection of triplet repeat sequences in yeast artificial chromosomes using oligonucleotide probes: application to the SCA1 region in 6p23
M Nemani, C Bellanné-Chantelot, D Cohen, et al.
Nucleic Acids Research
|
May 11, 1987
A subclone of the autosomal phosphoglycerate kinase pseudogene (HGM8 gene symbol PGK1P2), localized to 6p23-q12, detects moderately polymorphic RFLP
H Blanché, P Szabo, D Cohen, et al.
Pediatrics
|
April 1, 1970
Cytogenetic analysis of a boy with the XXXY syndrome: origin of the X-chromosomes
R M Greenstein, D J Harris, L Luzzatti, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1980
Maternal inheritance of human mitochondrial DNA
R E Giles, H Blanc, H M Cann, et al.
Archives of Dermatology
|
February 1, 1972
The genetics of psoriasis
W Watson, H M Cann, E M Farber, et al.
Human Molecular Genetics
|
January 1, 1993
A short tandem repeat polymorphism at the endothelin 1 (EDN1) locus
J C Pages, C Drieu, H Blanché, et al.
Tissue Antigens
|
January 1, 1973
Genetic structure of the HL-A system in a Nahua Indian population in Mexico
H M Cann, K K Kidd, R Lisker, et al.
Prenatal Diagnosis
|
January 1, 1981
Detection and isolation of fetal cells from maternal blood using the flourescence-activated cell sorter (FACS)
G M Iverson, D W Bianchi, H M Cann, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1983
Polymorphic restriction endonuclease fragment segregates and correlates with the gene for HLA-B8
H M Cann, L Ascanio, P Paul, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
Nucleic Acids Research
|
February 25, 1988
A fragment of the human c-Ki-ras1 pseudogene (HGM9 gene symbol KRAS1P), localized to 6p12-p11, detects 3 allele, RFLP
H Blanché, E H Chang, J Dausset, et al.
Cytogenetics and Cell Genetics
|
January 1, 1996
Detection of triplet repeat sequences in yeast artificial chromosomes using oligonucleotide probes: application to the SCA1 region in 6p23
M Nemani, C Bellanné-Chantelot, D Cohen, et al.
Nucleic Acids Research
|
May 11, 1987
A subclone of the autosomal phosphoglycerate kinase pseudogene (HGM8 gene symbol PGK1P2), localized to 6p23-q12, detects moderately polymorphic RFLP
H Blanché, P Szabo, D Cohen, et al.
Pediatrics
|
April 1, 1970
Cytogenetic analysis of a boy with the XXXY syndrome: origin of the X-chromosomes
R M Greenstein, D J Harris, L Luzzatti, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1980
Maternal inheritance of human mitochondrial DNA
R E Giles, H Blanc, H M Cann, et al.
Archives of Dermatology
|
February 1, 1972
The genetics of psoriasis
W Watson, H M Cann, E M Farber, et al.
Human Molecular Genetics
|
January 1, 1993
A short tandem repeat polymorphism at the endothelin 1 (EDN1) locus
J C Pages, C Drieu, H Blanché, et al.
Tissue Antigens
|
January 1, 1973
Genetic structure of the HL-A system in a Nahua Indian population in Mexico
H M Cann, K K Kidd, R Lisker, et al.
Prenatal Diagnosis
|
January 1, 1981
Detection and isolation of fetal cells from maternal blood using the flourescence-activated cell sorter (FACS)
G M Iverson, D W Bianchi, H M Cann, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1983
Polymorphic restriction endonuclease fragment segregates and correlates with the gene for HLA-B8
H M Cann, L Ascanio, P Paul, et al.
Page
of 5