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N Niikawa

Showing results (51-60 of 274) with videos related to

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Nucleic Acids Research|September 11, 1991
A BsaBI RFLP detected for probe pML34 [D15S9] on chromosome 15qJ Hamabe, S Saitoh, N Niikawa
American Journal of Medical Genetics|May 1, 1990
A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibsH Tonoki, T Kishino, N Niikawa
The Japanese Journal of Human Genetics|March 1, 1997
Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1K Nishiwaki, N Niikawa, M Ishikawa
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1984
The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infantsY Fukushima, N Niikawa, Y Kuroki
Clinical Genetics|May 1, 1982
The dermatoglyphic pattern of the Kabuki make-up syndromeN Niikawa, Y Kuroki, T Kajii
Nucleic Acids Research|November 25, 1990
Use of psoralen as extinguisher of contaminated DNA in PCRY Jinno, K Yoshiura, N Niikawa
American Journal of Medical Genetics|December 4, 1995
Confirmation of Down syndrome critical region by FISH analysis in a patient with add(21) (p11)N Matsumoto, N Niikawa, M Mikawa
American Journal of Medical Genetics|November 1, 1985
The "Michelin tire baby" syndrome--an autosomal dominant traitN Niikawa, S Ishikiriyama, T Shikimani
American Journal of Medical Genetics|December 11, 1996
De novo balanced translocation (6;18)(q21;q21.3 or q22) [corrected] in a patient with heterotaxiaR Kato, Y Yamada, N Niikawa
Journal of Medical Genetics|April 1, 1997
A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type IT Sasaki, H Tonoki, H Soejima, et al.
Pageof 28

Showing results (51-60 of 274) with videos related to

Sort By:
Pageof 28
Nucleic Acids Research|September 11, 1991
A BsaBI RFLP detected for probe pML34 [D15S9] on chromosome 15qJ Hamabe, S Saitoh, N Niikawa
American Journal of Medical Genetics|May 1, 1990
A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibsH Tonoki, T Kishino, N Niikawa
The Japanese Journal of Human Genetics|March 1, 1997
Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1K Nishiwaki, N Niikawa, M Ishikawa
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|March 1, 1984
The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infantsY Fukushima, N Niikawa, Y Kuroki
Clinical Genetics|May 1, 1982
The dermatoglyphic pattern of the Kabuki make-up syndromeN Niikawa, Y Kuroki, T Kajii
Nucleic Acids Research|November 25, 1990
Use of psoralen as extinguisher of contaminated DNA in PCRY Jinno, K Yoshiura, N Niikawa
American Journal of Medical Genetics|December 4, 1995
Confirmation of Down syndrome critical region by FISH analysis in a patient with add(21) (p11)N Matsumoto, N Niikawa, M Mikawa
American Journal of Medical Genetics|November 1, 1985
The "Michelin tire baby" syndrome--an autosomal dominant traitN Niikawa, S Ishikiriyama, T Shikimani
American Journal of Medical Genetics|December 11, 1996
De novo balanced translocation (6;18)(q21;q21.3 or q22) [corrected] in a patient with heterotaxiaR Kato, Y Yamada, N Niikawa
Journal of Medical Genetics|April 1, 1997
A 4 Mb cryptic deletion associated with inv(8)(q13.1q24.11) in a patient with trichorhinophalangeal syndrome type IT Sasaki, H Tonoki, H Soejima, et al.
Pageof 28