Ogata T - Search Results

1

Complex genomic rearrangement in the SOX9 5' region in a patient with Pierre Robin sequence and hypoplastic left scapula.

Fukami M, Tsuchiya T, Takada S, Kanbara A, Asahara H, Igarashi A, Kamiyama Y, Nishimura G, Ogata T. Fukami M, et al. Among authors: ogata t. Am J Med Genet A. 2012 Jul;158A(7):1529-34. doi: 10.1002/ajmg.a.35308. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22529047

2

Oto-palato-digital syndrome, type II: evidence for defective intramembranous ossification.

Ogata T, Matsuo N, Nishimura G, Hajikano H. Ogata T, et al. Am J Med Genet. 1990 Jun;36(2):226-31. doi: 10.1002/ajmg.1320360217. Am J Med Genet. 1990. PMID: 2114799

3

FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes.

Rao E, Weiss B, Fukami M, Mertz A, Meder J, Ogata T, Heinrich U, Garcia-Heras J, Schiebel K, Rappold GA. Rao E, et al. Among authors: ogata t. Hum Genet. 1997 Aug;100(2):236-9. doi: 10.1007/s004390050497. Hum Genet. 1997. PMID: 9254856

4

Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.

Matsuo M, Muroya K, Kosaki K, Ishii T, Fukushima Y, Anzo M, Ogata T. Matsuo M, et al. Among authors: ogata t. Am J Med Genet. 1999 Sep 3;86(1):44-50. Am J Med Genet. 1999. PMID: 10440827 Review.

5

Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome.

Kosho T, Muroya K, Nagai T, Fujimoto M, Yokoya S, Sakamoto H, Hirano T, Terasaki H, Ohashi H, Nishimura G, Sato S, Matsuo N, Ogata T. Kosho T, et al. Among authors: ogata t. J Clin Endocrinol Metab. 1999 Dec;84(12):4613-21. doi: 10.1210/jcem.84.12.6289. J Clin Endocrinol Metab. 1999. PMID: 10599728

6

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.

Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T. Matsuo M, et al. Among authors: ogata t. Am J Med Genet. 2000 Apr 10;91(4):267-72. Am J Med Genet. 2000. PMID: 10766981 Review.

7

Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata.

Ikegawa S, Ohashi H, Ogata T, Honda A, Tsukahara M, Kubo T, Kimizuka M, Shimode M, Hasegawa T, Nishimura G, Nakamura Y. Ikegawa S, et al. Among authors: ogata t. Am J Med Genet. 2000 Oct 2;94(4):300-5. doi: 10.1002/1096-8628(20001002)94:4<300::aid-ajmg7>3.0.co;2-3. Am J Med Genet. 2000. PMID: 11038443 Review.

8

SHOX haploinsufficiency and overdosage: impact of gonadal function status.

Ogata T, Matsuo N, Nishimura G. Ogata T, et al. 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.

9

FISH analysis for apparently simple terminal deletions of the X chromosome: identification of hidden structural abnormalities.

Ogata T, Matsuo N, Fukushima Y, Saito M, Nose O, Miharu N, Uehara S, Ishizuka B. Ogata T, et al. Am J Med Genet. 2001 Dec 15;104(4):307-11. Am J Med Genet. 2001. PMID: 11754066

10

SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features.

Ogata T, Muroya K, Sasaki G, Nishimura G, Kitoh H, Hattori T. Ogata T, et al. J Clin Endocrinol Metab. 2002 Mar;87(3):1390-4. doi: 10.1210/jcem.87.3.8348. J Clin Endocrinol Metab. 2002. PMID: 11889214

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