Harada N - Search Results

1

Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.

Coêlho KE, Egashira M, Kato R, Fujimoto M, Matsumoto N, Rerkamnuaychoke B, Abe K, Harada N, Ohashi H, Fukushima Y, Niikawa N. Coêlho KE, et al. Among authors: harada n. Am J Med Genet. 1996 Jun 14;63(3):468-71. doi: 10.1002/(SICI)1096-8628(19960614)63:3<468::AID-AJMG10>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8737654

2

Trisomy 13/trisomy 18 mosaicism in an infant.

Abe K, Harada N, Itoh T, Hirakawa O, Niikawa N. Abe K, et al. Among authors: harada n. Clin Genet. 1996 Nov;50(5):300-3. doi: 10.1111/j.1399-0004.1996.tb02378.x. Clin Genet. 1996. PMID: 9007314

3

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. 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

4

Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.

Kato R, Kishibayashi J, Shimokawa O, Harada N, Niikawa N, Matsumoto N. Kato R, et al. Among authors: harada n. Am J Med Genet. 2001 Dec 15;104(4):319-22. Am J Med Genet. 2001. PMID: 11754068

5

Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.

Deng HX, Yoshiura K, Dirks RW, Harada N, Hirota T, Tsukamoto K, Jinno Y, Niikawa N. Deng HX, et al. Among authors: harada n. Hum Genet. 1992 Apr;89(1):13-7. doi: 10.1007/BF00207034. Hum Genet. 1992. PMID: 1577461

6

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. Among authors: harada n. Hum Genet. 1991 Sep;87(5):561-6. doi: 10.1007/BF00209012. Hum Genet. 1991. PMID: 1680787

7

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: harada n. Am J Med Genet. 1991 Oct 1;41(1):54-63. doi: 10.1002/ajmg.1320410116. Am J Med Genet. 1991. PMID: 1683159

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: harada n. Am J Med Genet. 1989 Aug;33(4):505-7. doi: 10.1002/ajmg.1320330419. Am J Med Genet. 1989. PMID: 2596512

9

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: harada n. Am J Med Genet. 1994 Feb 15;49(4):428-30. doi: 10.1002/ajmg.1320490415. Am J Med Genet. 1994. PMID: 8160738

10

Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence.

Yamauchi M, Nagata S, Seki N, Toyama Y, Harada N, Niikawa N, Masuno I, Kajii T, Hori T. Yamauchi M, et al. Among authors: harada n. Clin Genet. 1993 Oct;44(4):169-72. doi: 10.1111/j.1399-0004.1993.tb03873.x. Clin Genet. 1993. PMID: 8261644

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