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Rinsho Byori. the Japanese Journal of Clinical Pathology
|
December 1, 1978
[Review on the gene, the fine structure of human chromosomes, and the application for prenatal diagnosis of cytogenetic examination (author's transl)]
J Furuyama, N Suehara
Mutation Research
|
July 1, 1988
Intragenic suppression in the uvrD gene of Escherichia coli. I. Temperature-sensitive uvrD mutations
Y Yamamoto, M Yabuki, J Furuyama
Clinical Genetics
|
December 1, 1990
An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA
M Yoshioka, Y Yamamoto, J Furuyama
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
June 1, 1974
Three cases of partial trisomy 9
H Fujita, T Abe, J Furuyama
Human Genetics
|
February 1, 1980
Reciprocal translocation t(5;6)(p13;q27) through three generations: case report of cri du chat syndrome
T Hashimoto, R Tsukino, H Chiyo, et al.
Cell Structure and Function
|
June 1, 1984
Cytidine deaminase levels in cultured mammalian cell lines measured by the growth tests and enzyme assays
K Ishii, H Sakamoto, J Furuyama, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy
|
February 1, 1988
[Recent trends in studies on carcinogenesis in familial adenomatous polyposis]
J Utsunomiya, Y Miki, T Kuroki, et al.
Journal of Reproductive Immunology
|
May 1, 1989
A testis-specific antigen of the C57BL/6 mouse
O Mikami, H Sakamoto, Y Yamamoto, et al.
Humangenetik
|
January 1, 1974
Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome
H Fujita, T Abe, K Yamamoto, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
September 1, 1970
G1 ring chromosome in a girl with red hair, harelip and cleft palate
H Fujita, T Kurose, Y Tanigawa, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 86) with videos related to
Sort By:
Page
of 9
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
December 1, 1978
[Review on the gene, the fine structure of human chromosomes, and the application for prenatal diagnosis of cytogenetic examination (author's transl)]
J Furuyama, N Suehara
Mutation Research
|
July 1, 1988
Intragenic suppression in the uvrD gene of Escherichia coli. I. Temperature-sensitive uvrD mutations
Y Yamamoto, M Yabuki, J Furuyama
Clinical Genetics
|
December 1, 1990
An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA
M Yoshioka, Y Yamamoto, J Furuyama
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
June 1, 1974
Three cases of partial trisomy 9
H Fujita, T Abe, J Furuyama
Human Genetics
|
February 1, 1980
Reciprocal translocation t(5;6)(p13;q27) through three generations: case report of cri du chat syndrome
T Hashimoto, R Tsukino, H Chiyo, et al.
Cell Structure and Function
|
June 1, 1984
Cytidine deaminase levels in cultured mammalian cell lines measured by the growth tests and enzyme assays
K Ishii, H Sakamoto, J Furuyama, et al.
Gan to Kagaku Ryoho. Cancer & Chemotherapy
|
February 1, 1988
[Recent trends in studies on carcinogenesis in familial adenomatous polyposis]
J Utsunomiya, Y Miki, T Kuroki, et al.
Journal of Reproductive Immunology
|
May 1, 1989
A testis-specific antigen of the C57BL/6 mouse
O Mikami, H Sakamoto, Y Yamamoto, et al.
Humangenetik
|
January 1, 1974
Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome
H Fujita, T Abe, K Yamamoto, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics
|
September 1, 1970
G1 ring chromosome in a girl with red hair, harelip and cleft palate
H Fujita, T Kurose, Y Tanigawa, et al.
Page
of 9