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Human Genetics
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January 1, 1984
Origin of extra chromosome in Patau syndrome
S Ishikiriyama, N Niikawa
Nucleic Acids Research
|
May 25, 1990
PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNA
H 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 son
H 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 tissues
K Tsukamoto, Y Nakamura, N Niikawa
Human Genetics
|
December 29, 1977
Origin of acrocentric trisomies in spontaneous abortuses
N Niikawa, E Merotto, T Kajii
The Japanese Journal of Human Genetics
|
March 1, 1997
Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3
R Kato, N Matsumoto, N Niikawa
Human Genetics
|
July 1, 1989
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome
K 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 girl
K Abe, N Niikawa, H Sasaki
Page
of 28
Search research articles
Search
Showing results (41-50 of 274) with videos related to
Sort By:
Page
of 28
Human Genetics
|
January 1, 1984
Origin of extra chromosome in Patau syndrome
S Ishikiriyama, N Niikawa
Nucleic Acids Research
|
May 25, 1990
PvuII RFLPs in the DMD gene detected by a subclone (cDMD1a) of the cDNA
H 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 son
H 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 tissues
K Tsukamoto, Y Nakamura, N Niikawa
Human Genetics
|
December 29, 1977
Origin of acrocentric trisomies in spontaneous abortuses
N Niikawa, E Merotto, T Kajii
The Japanese Journal of Human Genetics
|
March 1, 1997
Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3
R Kato, N Matsumoto, N Niikawa
Human Genetics
|
July 1, 1989
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome
K 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 girl
K Abe, N Niikawa, H Sasaki
Page
of 28