Harada 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. 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

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

3

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

4

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

5

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

6

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

7

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

8

Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma.

Matsumoto T, Kinoshita E, Maeda H, Niikawa N, Kurosaki N, Harada N, Yun K, Sawai T, Aoki S, Kondoh T, et al. Matsumoto T, et al. Among authors: harada n. Jpn J Hum Genet. 1994 Jun;39(2):225-34. doi: 10.1007/BF01876842. Jpn J Hum Genet. 1994. PMID: 8086640

9

EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3).

Akita S, Kuratomi H, Abe K, Harada N, Mukae N, Niikawa N. Akita S, et al. Among authors: harada n. Clin Dysmorphol. 1993 Jan;2(1):62-7. Clin Dysmorphol. 1993. PMID: 8298740

10

[Trisomy 13 syndrome (Patau syndrome), trisomy 18 syndrome (Edwards syndrome), Down syndrome (trisomy 21 syndrome), Turner syndrome (XO gonadal dysgenesis)].

Harada N, Niikawa N. Harada N, et al. Ryoikibetsu Shokogun Shirizu. 1996;(15):198-201. Ryoikibetsu Shokogun Shirizu. 1996. PMID: 9047985 Review. Japanese. No abstract available.

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