Matsuo N - Search Results

1

Short stature in a girl with partial monosomy of the pseudoautosomal region distal to DXYS15: further evidence for the assignment of the critical region for a pseudoautosomal growth gene(s).

Ogata T, Yoshizawa A, Muroya K, Matsuo N, Fukushima Y, Rappold G, Yokoya S. Ogata T, et al. Among authors: matsuo n. J Med Genet. 1995 Oct;32(10):831-4. doi: 10.1136/jmg.32.10.831. J Med Genet. 1995. PMID: 8558568 Free PMC article.

2

Chromosomal localisation of a Y specific growth gene(s).

Ogata T, Tomita K, Hida A, Matsuo N, Nakahori Y, Nakagome Y. Ogata T, et al. Among authors: matsuo n. J Med Genet. 1995 Jul;32(7):572-5. doi: 10.1136/jmg.32.7.572. J Med Genet. 1995. PMID: 7562976 Free PMC article.

3

Refinement of the locus for X-linked recessive chondrodysplasia punctata.

Muroya K, Ogata T, Rappold G, Klink A, Nakahori Y, Fukushima Y, Aizu K, Matsuo N. Muroya K, et al. Among authors: matsuo n. Hum Genet. 1995 May;95(5):577-80. doi: 10.1007/BF00223874. Hum Genet. 1995. PMID: 7759082

4

Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Ogata T, Matsuo N. Ogata T, et al. Among authors: matsuo n. Hum Genet. 1995 Jun;95(6):607-29. doi: 10.1007/BF00209476. Hum Genet. 1995. PMID: 7789944 Review.

5

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locus.

Muroya K, Ogata T, Matsuo N, Nagai T, Franco B, Ballabio A, Rappold G, Sakura N, Fukushima Y. Muroya K, et al. Among authors: matsuo n. Am J Med Genet. 1996 Sep 6;64(4):583-7. doi: 10.1002/(SICI)1096-8628(19960906)64:4<583::AID-AJMG11>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870926

6

The Y specific growth gene(s): how does it promote stature?

Ogata T, Matsuo N. Ogata T, et al. Among authors: matsuo n. J Med Genet. 1997 Apr;34(4):323-5. doi: 10.1136/jmg.34.4.323. J Med Genet. 1997. PMID: 9138158 Free PMC article.

7

Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p.

Ogata T, Muroya K, Matsuo N, Hata J, Fukushima Y, Suzuki Y. Ogata T, et al. Among authors: matsuo n. J Med Genet. 1997 Apr;34(4):331-4. doi: 10.1136/jmg.34.4.331. J Med Genet. 1997. PMID: 9138160 Free PMC article.

8

Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern.

Ogata T, Wakui K, Muroya K, Ohashi H, Matsuo N, Brown DM, Ishii T, Fukushima Y. Ogata T, et al. Among authors: matsuo n. Hum Genet. 1998 Jul;103(1):51-6. doi: 10.1007/s004390050782. Hum Genet. 1998. PMID: 9737776 Review.

9

Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11.

Muroya K, Kinoshita E, Kamimaki T, Matsuo N, Yorifugi T, Ogata T. Muroya K, et al. Among authors: matsuo n. J Med Genet. 1999 Mar;36(3):187-91. J Med Genet. 1999. PMID: 10204842 Free PMC article.

10

SHOX haploinsufficiency and overdosage: impact of gonadal function status.

Ogata T, Matsuo N, Nishimura G. Ogata T, et al. Among authors: matsuo n. J Med Genet. 2001 Jan;38(1):1-6. doi: 10.1136/jmg.38.1.1. J Med Genet. 2001. PMID: 11134233 Free PMC article. Review.

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