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N Niikawa

Showing results (81-90 of 274) with videos related to

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Human Genetics|June 9, 1978
Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblingsN Niikawa, I Matsuda, T Ohsawa, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1972
A case of congenital asymmetry associated with trisomy 18 mosaicismM Sasaki, S I Sonta, N Niikawa, et al.
Human Genetics|August 1, 1986
A further improved method for identifying heteromorphism of acrocentric chromosomesT Kamei, S Lee-Okimoto, M Sohda, et al.
Annales De Genetique|January 1, 1981
Ring chromosome 11 [46,XX,r(11) (p15q25)] associated with clinical features of the 11q- syndromeN Niikawa, Y Jinno, T Tomiyasu, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1989
Micro extraction of DNA from whole blood and amniocytesT Hirota, T Kondoh, T Matsumoto, et al.
Journal of the Neurological Sciences|April 1, 1993
Dystrophin isoforms expressed in the mouse retinaT Tamura, K Yoshioka, Y Jinno, et al.
The Japanese Journal of Human Genetics|March 1, 1996
Physical map of a YAC contig containing the region of the human gene (HYRC) complementing hyper-radiosensitivity of the scid mouse mutationY Watanabe, N Matsumoto, T Ohta, et al.
Journal of Assisted Reproduction and Genetics|October 1, 1996
A partial hydatidiform mole with 2N/3N mosaicism identified by molecular analysisY Ikeda, Y Jinno, H Masuzaki, et al.
Clinical Genetics|February 1, 1991
XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardationT Matsumoto, K Taku, T Miike, et al.
American Journal of Medical Genetics|April 6, 1999
Mutchinick syndrome in a Japanese girlH Tonoki, T Hattori, H Kamoshida, et al.
Pageof 28

Showing results (81-90 of 274) with videos related to

Sort By:
Pageof 28
Human Genetics|June 9, 1978
Familial occurrence of a syndrome with mental retardation, nasal hypoplasia, peripheral dysostosis, and blue eyes in Japanese siblingsN Niikawa, I Matsuda, T Ohsawa, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1972
A case of congenital asymmetry associated with trisomy 18 mosaicismM Sasaki, S I Sonta, N Niikawa, et al.
Human Genetics|August 1, 1986
A further improved method for identifying heteromorphism of acrocentric chromosomesT Kamei, S Lee-Okimoto, M Sohda, et al.
Annales De Genetique|January 1, 1981
Ring chromosome 11 [46,XX,r(11) (p15q25)] associated with clinical features of the 11q- syndromeN Niikawa, Y Jinno, T Tomiyasu, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1989
Micro extraction of DNA from whole blood and amniocytesT Hirota, T Kondoh, T Matsumoto, et al.
Journal of the Neurological Sciences|April 1, 1993
Dystrophin isoforms expressed in the mouse retinaT Tamura, K Yoshioka, Y Jinno, et al.
The Japanese Journal of Human Genetics|March 1, 1996
Physical map of a YAC contig containing the region of the human gene (HYRC) complementing hyper-radiosensitivity of the scid mouse mutationY Watanabe, N Matsumoto, T Ohta, et al.
Journal of Assisted Reproduction and Genetics|October 1, 1996
A partial hydatidiform mole with 2N/3N mosaicism identified by molecular analysisY Ikeda, Y Jinno, H Masuzaki, et al.
Clinical Genetics|February 1, 1991
XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardationT Matsumoto, K Taku, T Miike, et al.
American Journal of Medical Genetics|April 6, 1999
Mutchinick syndrome in a Japanese girlH Tonoki, T Hattori, H Kamoshida, et al.
Pageof 28