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Human Genetics
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September 12, 2000
Congenital cataracts: gene mapping
W He, S Li
Human Genetics
|
September 27, 2015
Association between telomere length and chromosome 21 nondisjunction in the oocyte
I Albizua, B L Rambo-Martin, E G Allen, et al.
Human Genetics
|
November 1, 1991
Genotypic analysis of families with lactate dehydrogenase A (M) deficiency by selective DNA amplification
M Maekawa, K Sudo, S S Li, et al.
Human Genetics
|
January 1, 1994
Population screening of lactate dehydrogenase deficiencies in Fukuoka Prefecture in Japan and molecular characterization of three independent mutations in the lactate dehydrogenase-B(H) gene
M Maekawa, K Sudo, K Nagura, et al.
Human Genetics
|
June 1, 1993
Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunit
M Maekawa, K Sudo, M Kitajima, et al.
Human Genetics
|
March 1, 1993
Detection and characterization of new genetic mutations in individuals heterozygous for lactate dehydrogenase-B(H) deficiency using DNA conformation polymorphism analysis and silver staining
M Maekawa, K Sudo, M Kitajima, et al.
Human Genetics
|
May 1, 1992
Molecular characterization of genetic mutations in human lactate dehydrogenase (LDH) B (H) variant
K Sudo, M Maekawa, A Tomonaga, et al.
Human Genetics
|
April 1, 1994
SRVX, a sex reversing locus in Xp21.2-->p22.11
P Arn, H Chen, C M Tuck-Muller, et al.
Human Genetics
|
July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature
C M Tuck-Muller, H Chen, J E Martínez, et al.
Human Genetics
|
May 14, 1999
Molecular characterization of germline mutations in the BRCA1 and BRCA2 genes from breast cancer families in Taiwan
S S Li, H M Tseng, T P Yang, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Human Genetics
|
September 12, 2000
Congenital cataracts: gene mapping
W He, S Li
Human Genetics
|
September 27, 2015
Association between telomere length and chromosome 21 nondisjunction in the oocyte
I Albizua, B L Rambo-Martin, E G Allen, et al.
Human Genetics
|
November 1, 1991
Genotypic analysis of families with lactate dehydrogenase A (M) deficiency by selective DNA amplification
M Maekawa, K Sudo, S S Li, et al.
Human Genetics
|
January 1, 1994
Population screening of lactate dehydrogenase deficiencies in Fukuoka Prefecture in Japan and molecular characterization of three independent mutations in the lactate dehydrogenase-B(H) gene
M Maekawa, K Sudo, K Nagura, et al.
Human Genetics
|
June 1, 1993
Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunit
M Maekawa, K Sudo, M Kitajima, et al.
Human Genetics
|
March 1, 1993
Detection and characterization of new genetic mutations in individuals heterozygous for lactate dehydrogenase-B(H) deficiency using DNA conformation polymorphism analysis and silver staining
M Maekawa, K Sudo, M Kitajima, et al.
Human Genetics
|
May 1, 1992
Molecular characterization of genetic mutations in human lactate dehydrogenase (LDH) B (H) variant
K Sudo, M Maekawa, A Tomonaga, et al.
Human Genetics
|
April 1, 1994
SRVX, a sex reversing locus in Xp21.2-->p22.11
P Arn, H Chen, C M Tuck-Muller, et al.
Human Genetics
|
July 1, 1995
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature
C M Tuck-Muller, H Chen, J E Martínez, et al.
Human Genetics
|
May 14, 1999
Molecular characterization of germline mutations in the BRCA1 and BRCA2 genes from breast cancer families in Taiwan
S S Li, H M Tseng, T P Yang, et al.
Page
of 1