Harada N - Search Results

1

A 4q21-q22 deletion in a girl with severe growth retardation.

Harada N, Nagai T, Shimokawa O, Niikawa N, Matsumoto N. Harada N, et al. Clin Genet. 2002 Mar;61(3):226-8. doi: 10.1034/j.1399-0004.2002.610311.x. Clin Genet. 2002. PMID: 12000367 No abstract available.

2

A 4-Mb critical region for intrauterine growth retardation at 15q26.

Harada N, Shimokawa O, Nagai T, Kato R, Kondoh T, Niikawa N, Matsumoto N. Harada N, et al. Clin Genet. 2002 Oct;62(4):340-2. doi: 10.1034/j.1399-0004.2002.620416.x. Clin Genet. 2002. PMID: 12372065 No abstract available.

3

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

4

XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation.

Matsumoto T, Taku K, Miike T, Harada N, Niikawa N. Matsumoto T, et al. Among authors: harada n. Clin Genet. 1991 Feb;39(2):156-8. doi: 10.1111/j.1399-0004.1991.tb03004.x. Clin Genet. 1991. PMID: 2015697 No abstract available.

5

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

6

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

7

Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature.

Uehara S, Hanew K, Harada N, Yamamori S, Nata M, Niikawa N, Okamura K. Uehara S, et al. Among authors: harada n. Am J Med Genet. 2001 Mar 15;99(3):196-9. doi: 10.1002/1096-8628(20010315)99:3<196::aid-ajmg1157>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11241489

8

Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions.

Nagai T, Matsumoto N, Kurotaki N, Harada N, Niikawa N, Ogata T, Imaizumi K, Kurosawa K, Kondoh T, Ohashi H, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Yokoyama T, Uetake K, Sakazume S, Fukushima Y, Naritomi K. Nagai T, et al. Among authors: harada n. J Med Genet. 2003 Apr;40(4):285-9. doi: 10.1136/jmg.40.4.285. J Med Genet. 2003. PMID: 12676901 Free PMC article. No abstract available.

9

Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation.

Harada N, Hatchwell E, Okamoto N, Tsukahara M, Kurosawa K, Kawame H, Kondoh T, Ohashi H, Tsukino R, Kondoh Y, Shimokawa O, Ida T, Nagai T, Fukushima Y, Yoshiura K, Niikawa N, Matsumoto N. Harada N, et al. J Med Genet. 2004 Feb;41(2):130-6. doi: 10.1136/jmg.2003.014639. J Med Genet. 2004. PMID: 14757861 Free PMC article. No abstract available.

10

Visser R, Shimokawa O, Harada N, Niikawa N, Matsumoto N. Visser R, et al. Among authors: harada n. J Med Genet. 2005 Nov;42(11):e66. doi: 10.1136/jmg.2005.034355. J Med Genet. 2005. PMID: 16272258 Free PMC article.

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