Niikawa N - Search Results

1

Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus.

Harada N, Abe K, Nishimura T, Sasaki K, Ishikawa M, Fujimoto M, Matsumoto T, Niikawa N. Harada N, et al. Among authors: niikawa n. Am J Med Genet. 1998 Feb 3;75(4):432-7. doi: 10.1002/(sici)1096-8628(19980203)75:4<432::aid-ajmg17>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482654

2

Origin and mechanisms of formation of fetus-in-fetu: two cases with genotype and methylation analyses.

Miura S, Miura K, Yamamoto T, Yamanaka M, Saito K, Hirabuki T, Kurosawa K, Harada N, Ishizaki-Yamasaki Y, Matsumoto N, Hirahara F, Yoshiura K, Masuzaki H, Niikawa N. Miura S, et al. Among authors: niikawa n. Am J Med Genet A. 2006 Aug 15;140(16):1737-43. doi: 10.1002/ajmg.a.31362. Am J Med Genet A. 2006. PMID: 16835914

3

Identification of de novo chromosome rearrangements: five cases analyzed with differential chromosome painting.

Ida T, Harada N, Abe K, Kondoh T, Yoshinaga M, Maki T, Niikawa N. Ida T, et al. Among authors: niikawa n. Am J Med Genet. 2002 Mar 15;108(3):182-6. doi: 10.1002/ajmg.10257. Am J Med Genet. 2002. PMID: 11891682

4

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2.

Niikawa N, Deng HX, Abe K, Harada N, Okada T, Tsuchiya H, Akaboshi I, Matsuda I, Fukushima Y, Kaneko Y, et al. Niikawa N, et al. Hum Genet. 1991 Sep;87(5):561-6. doi: 10.1007/BF00209012. Hum Genet. 1991. PMID: 1680787

5

Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.

Hamabe J, Fukushima Y, Harada N, Abe K, Matsuo N, Nagai T, Yoshioka A, Tonoki H, Tsukino R, Niikawa N. Hamabe J, et al. Among authors: niikawa n. Am J Med Genet. 1991 Oct 1;41(1):54-63. doi: 10.1002/ajmg.1320410116. Am J Med Genet. 1991. PMID: 1683159

6

Parental origin and mechanism of formation of X chromosome structural abnormalities: four cases determined with RFLPs.

Deng HX, Xia JH, Ishikawa M, Niikawa N. Deng HX, et al. Among authors: niikawa n. Jinrui Idengaku Zasshi. 1990 Sep;35(3):245-51. doi: 10.1007/BF01876853. Jinrui Idengaku Zasshi. 1990. PMID: 1979996

7

Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome.

Abe K, Kajii T, Niikawa N. Abe K, et al. Among authors: niikawa n. Hum Genet. 1989 Jul;82(4):313-6. doi: 10.1007/BF00273988. Hum Genet. 1989. PMID: 2525515

8

Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).

Ishikiriyama S, Tonoki H, Shibuya Y, Chin S, Harada N, Abe K, Niikawa N. Ishikiriyama S, et al. Among authors: niikawa n. Am J Med Genet. 1989 Aug;33(4):505-7. doi: 10.1002/ajmg.1320330419. Am J Med Genet. 1989. PMID: 2596512

9

Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.

Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N. Kubota T, et al. Among authors: niikawa n. Am J Med Genet. 1994 Feb 15;49(4):378-83. doi: 10.1002/ajmg.1320490405. Am J Med Genet. 1994. PMID: 7909196

10

Case of 46,XX/47,XY, +21 chimerism in a newborn infant with ambiguous genitalia.

Sawai T, Yoshimoto M, Kinoshita E, Baba T, Matsumoto T, Tsuji Y, Fukuda S, Harada N, Niikawa N. Sawai T, et al. Among authors: niikawa n. Am J Med Genet. 1994 Feb 15;49(4):428-30. doi: 10.1002/ajmg.1320490415. Am J Med Genet. 1994. PMID: 8160738

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