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N Niikawa

Showing results (41-50 of 274) with videos related to

Pageof 28
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Human Genetics|January 1, 1984
Origin of extra chromosome in Patau syndromeS Ishikiriyama, N Niikawa
Nucleic Acids Research|May 25, 1990
PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNAH X Deng, N Niikawa
Nucleic Acids Research|August 25, 1991
An ApaI RFLP for the human porphobilinogen deaminase gene (PBGD)J Hamabe, H Irifune, N Niikawa
Human Genetics|January 1, 1981
13S+. Giant satellites or de novo rearrangement?K Imaizumi, T Kajii, N Niikawa
American Journal of Medical Genetics|April 1, 1988
Cryptomicrotia and short, stubby fingers with excess fingertip arch patterns in a mother and sonH Tonoki, T Ohura, N Niikawa
Human Genetics|March 1, 1994
Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissuesK Tsukamoto, Y Nakamura, N Niikawa
Human Genetics|December 29, 1977
Origin of acrocentric trisomies in spontaneous abortusesN Niikawa, E Merotto, T Kajii
The Japanese Journal of Human Genetics|March 1, 1997
Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3R Kato, N Matsumoto, N Niikawa
Human Genetics|July 1, 1989
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndromeK Abe, T Kajii, N Niikawa
American Journal of Diseases of Children (1960)|July 1, 1979
Zollinger-Ellison syndrome with Marden-Walker syndrome. Association of two rare diseases in a 5-year-old girlK Abe, N Niikawa, H Sasaki
Pageof 28

Showing results (41-50 of 274) with videos related to

Sort By:
Pageof 28
Human Genetics|January 1, 1984
Origin of extra chromosome in Patau syndromeS Ishikiriyama, N Niikawa
Nucleic Acids Research|May 25, 1990
PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNAH X Deng, N Niikawa
Nucleic Acids Research|August 25, 1991
An ApaI RFLP for the human porphobilinogen deaminase gene (PBGD)J Hamabe, H Irifune, N Niikawa
Human Genetics|January 1, 1981
13S+. Giant satellites or de novo rearrangement?K Imaizumi, T Kajii, N Niikawa
American Journal of Medical Genetics|April 1, 1988
Cryptomicrotia and short, stubby fingers with excess fingertip arch patterns in a mother and sonH Tonoki, T Ohura, N Niikawa
Human Genetics|March 1, 1994
Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissuesK Tsukamoto, Y Nakamura, N Niikawa
Human Genetics|December 29, 1977
Origin of acrocentric trisomies in spontaneous abortusesN Niikawa, E Merotto, T Kajii
The Japanese Journal of Human Genetics|March 1, 1997
Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3R Kato, N Matsumoto, N Niikawa
Human Genetics|July 1, 1989
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndromeK Abe, T Kajii, N Niikawa
American Journal of Diseases of Children (1960)|July 1, 1979
Zollinger-Ellison syndrome with Marden-Walker syndrome. Association of two rare diseases in a 5-year-old girlK Abe, N Niikawa, H Sasaki
Pageof 28