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Norio Niikawa

Veröffentlichungen von Norio Niikawa zu Niikawa, Norio ->
weitere Veröffentlichungen von Norio Niikawa:
Prader-Willi syndrome: Consideration of a question in its clinical, cytogenetic and molecular aspects (1990)
Symposium III. Recent Advances in Molecular Cytogenetics (1992)
Genomic imprinting and its relevance to genetic diseases (1996)
A triploid human abortus due to dispermy (1974)
Sequential Q- and acridine orange-marker technique (1975)
Whole-arm translocation between homologous chromosomes 7 in a woman with successive spontaneous abortions (1983)
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 infants (1984)
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome (1989)
Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues (1994)
Origin of acrocentric trisomies in spontaneous abortuses (1977)
A further improved method for identifying heteromorphism of acrocentric chromosomes (1986)
Origin of the extra chromosome in trisomy 18 (1988)
Satellited chromosome 9 in a boy with multiple anomalies (1989)
Micro extraction of DNA from whole blood and amniocytes (1989)
Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction (1991)
Veröffentlichungen zu Niikawa, Norio
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1
Niikawa, Norio Prader-Willi syndrome: Consideration of a question in its clinical, cytogenetic and molecular aspects
in: Journal of human genetics , ISSN 1435-232X, Vol. 35 (1. 1990), p. 19-19
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1990
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2
Niikawa, Norio Symposium III. Recent Advances in Molecular Cytogenetics
in: Journal of human genetics , ISSN 1435-232X, Vol. 37 (1. 1992), p. 27-105
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1992
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3
Niikawa, Norio Genomic imprinting and its relevance to genetic diseases
in: Journal of human genetics , ISSN 1435-232X, Vol. 41 (4. 1996), p. 351-361
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1996
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4
Niikawa, Norio, Kajii, Tadashi A triploid human abortus due to dispermy
in: Human genetics , ISSN 1432-1203, Vol. 24 (3. 1974), p. 261-264
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1974
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5
Niikawa, Norio, Kajii, Tadashi Sequential Q- and acridine orange-marker technique
in: Human genetics , ISSN 1432-1203, Vol. 30 (1. 1975), p. 83-90
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1975
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6
Niikawa, Norio, Ishikawa, Mutsuo Whole-arm translocation between homologous chromosomes 7 in a woman with successive spontaneous abortions
in: Human genetics , ISSN 1432-1203, Vol. 63 (1. 1983), p. 85-86
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1983
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7
Fukushima, Yoshimitsu, Niikawa, Norio, ... 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 infants
in: Journal of human genetics , ISSN 1435-232X, Vol. 29 (1. 1984), p. 1-6
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1984
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8
Abe, Kyohko, Kajii, Tadashi, ... Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome
in: Human genetics , ISSN 1432-1203, Vol. 82 (4. 1989), p. 313-316
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1989
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9
Tsukamoto, Kazuhiro, Nakamura, Yusuke, ... Isolation of two isoforms of the PAX3 gene transcripts and their tissue-specific alternative expression in human adult tissues
in: Human genetics , ISSN 1432-1203, Vol. 93 (3. 1994), p. 270-274
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1994
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10
Niikawa, Norio, Merotto, Elisabeth, ... Origin of acrocentric trisomies in spontaneous abortuses
in: Human genetics , ISSN 1432-1203, Vol. 40 (1. 1977), p. 73-78
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1977
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11
Kamei, Tsutomu, Lee-Okimoto, Sei, ... A further improved method for identifying heteromorphism of acrocentric chromosomes
in: Human genetics , ISSN 1432-1203, Vol. 73 (4. 1986), p. 368-371
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1986
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12
Kondoh, Tatsuro, Tonoki, Hidefumi, ... Origin of the extra chromosome in trisomy 18
in: Human genetics , ISSN 1432-1203, Vol. 79 (4. 1988), p. 377-378
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1988
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13
Harada, Naoki, Abe, Kyohko, ... Satellited chromosome 9 in a boy with multiple anomalies
in: Journal of human genetics , ISSN 1435-232X, Vol. 34 (4. 1989), p. 297-305
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1989
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14
Hirota, Tetsuya, Kondoh, Tatsuro, ... Micro extraction of DNA from whole blood and amniocytes
in: Journal of human genetics , ISSN 1435-232X, Vol. 34 (3. 1989), p. 217-223
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1989
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15
Fujishita, Satoshi, Shibuya, Noritoshi, ... Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction
in: Journal of human genetics , ISSN 1435-232X, Vol. 36 (4. 1991), p. 317-324
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1991
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16
Miyatake, Satoko, Ikeda, Yuichiro, ... Two polymorphicAvaI andHhaI sites in a differentially methylated region of the human H19 gene
in: Journal of human genetics , ISSN 1435-232X, Vol. 41 (2. 1996), p. 253-255
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1996
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17
Watanabe, Yoriko, Matsumoto, Naomichi, ... Physical map of a YAC contig containing the region of the human gene (HYRC) complementing hyper-radiosensitivity of the scid mouse mutation
in: Journal of human genetics , ISSN 1435-232X, Vol. 41 (1. 1996), p. 149-158
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1996
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18
Ikeda, Yuichiro, Jinno, Yoshihiro, ... A partial hydatidiform mole with 2N/3N mosaicism identified by molecular analysis
in: Journal of assisted reproduction and genetics , ISSN 1573-7330, Vol. 13 (9. 1996), p. 739-744
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1996
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19
Miura, Kiyonori, Masuzaki, Hideaki, ... A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5
in: Journal of human genetics , ISSN 1435-232X, Vol. 43 (4. 1998), p. 283-284
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1998
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20
Jinno, Yoshihiro, Yun, Kankatsu, ... Mosaic and polymorphic imprinting of the WT1 gene in humans
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 6, No. 3 (1994), p. 305-309
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1994