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T Motegi

Showing results (11-20 of 28) with videos related to

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Human Genetics|January 1, 1982
Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: the assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of itT Motegi, M Komatsu, Y Nakazato, et al.
Journal of Medical Genetics|February 1, 1985
De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cellsT Motegi, K Watanabe, N Nakamura, et al.
Journal of Biotechnology|May 19, 2000
Electrically stimulated induction of hsp70 gene expression in mouse astroglia and fibroblast cellsY Yanagida, A Mizuno, T Motegi, et al.
Human Genetics|October 31, 1978
18p-Mosaicism: case report and reviewT Motegi, A Ichikawa, M Noda, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|March 1, 1997
Aspergillus endocarditis in a leukemia patient diagnosed by a PCR assayY Kanda, H Akiyama, Y Onozawa, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|February 26, 2000
[Interstitial pneumonitis associated with Sweet's syndrome in the elderly]H Katsura, T Hara, T Motegi, et al.
Human Genetics|July 18, 1979
Short rib-polydactyly syndrome, Majewski type, in two male siblingsT Motegi, M Kusunoki, T Nishi, et al.
Pediatrics|April 1, 1977
Prepubertal XY gonadal dysgenesisK Isurugi, Y Aso, H Ishida, et al.
The Japanese Journal of Human Genetics|June 1, 1992
DNA analysis of two patients with a non-fluorescent Y chromosomeT Sekine, K Fukutani, T Motegi, et al.
Human Genetics|January 1, 1985
A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21T Motegi, M Ohuchi, C Ohtaki, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Human Genetics|January 1, 1982
Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: the assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of itT Motegi, M Komatsu, Y Nakazato, et al.
Journal of Medical Genetics|February 1, 1985
De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cellsT Motegi, K Watanabe, N Nakamura, et al.
Journal of Biotechnology|May 19, 2000
Electrically stimulated induction of hsp70 gene expression in mouse astroglia and fibroblast cellsY Yanagida, A Mizuno, T Motegi, et al.
Human Genetics|October 31, 1978
18p-Mosaicism: case report and reviewT Motegi, A Ichikawa, M Noda, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|March 1, 1997
Aspergillus endocarditis in a leukemia patient diagnosed by a PCR assayY Kanda, H Akiyama, Y Onozawa, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|February 26, 2000
[Interstitial pneumonitis associated with Sweet's syndrome in the elderly]H Katsura, T Hara, T Motegi, et al.
Human Genetics|July 18, 1979
Short rib-polydactyly syndrome, Majewski type, in two male siblingsT Motegi, M Kusunoki, T Nishi, et al.
Pediatrics|April 1, 1977
Prepubertal XY gonadal dysgenesisK Isurugi, Y Aso, H Ishida, et al.
The Japanese Journal of Human Genetics|June 1, 1992
DNA analysis of two patients with a non-fluorescent Y chromosomeT Sekine, K Fukutani, T Motegi, et al.
Human Genetics|January 1, 1985
A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21T Motegi, M Ohuchi, C Ohtaki, et al.
Pageof 3