Matsuo N - Search Results

1

Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata.

Hasegawa T, Ogata T, Hasegawa Y, Honda M, Nagai T, Fukushima Y, Nakahori Y, Matsuo N. Hasegawa T, et al. Among authors: matsuo n. Hum Genet. 1996 May;97(5):564-7. doi: 10.1007/BF02281861. Hum Genet. 1996. PMID: 8655131

2

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

3

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.

4

Further clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner stigmata.

Ogata T, Hasegawa T, Matsuo N. Ogata T, et al. Among authors: matsuo n. Hum Genet. 1997 Feb;99(2):290. doi: 10.1007/s004390050358. Hum Genet. 1997. PMID: 9048940 No abstract available.

5

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.

6

Proximal renal tubular acidosis associated with glycogen storage disease, type 9.

Nagai T, Matsuo N, Tsuchiya Y, Cho H, Hasegawa Y, Igarashi Y. Nagai T, et al. Among authors: matsuo n. Acta Paediatr Scand. 1988 May;77(3):460-3. doi: 10.1111/j.1651-2227.1988.tb10681.x. Acta Paediatr Scand. 1988. PMID: 3164568

7

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.

8

Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

Ogata T, Matsuo N. Ogata T, et al. Among authors: matsuo n. Hum Genet. 1993 Jul;91(6):551-62. doi: 10.1007/BF00205079. Hum Genet. 1993. PMID: 8340109

9

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.

10

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

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