Ogata T - Search Results

1

Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients.

Kawashima S, Nakamura A, Inoue T, Matsubara K, Horikawa R, Wakui K, Takano K, Fukushima Y, Tatematsu T, Mizuno S, Tsubaki J, Kure S, Matsubara Y, Ogata T, Fukami M, Kagami M. Kawashima S, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2018 Jun 1;103(6):2083-2088. doi: 10.1210/jc.2017-02780. J Clin Endocrinol Metab. 2018. PMID: 29878129

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: ogata t. Hum Genet. 1995 May;95(5):577-80. doi: 10.1007/BF00223874. Hum Genet. 1995. PMID: 7759082

3

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. 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.

4

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. 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.

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. Hum Genet. 1998 Jul;103(1):51-6. doi: 10.1007/s004390050782. Hum Genet. 1998. PMID: 9737776 Review.

6

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.

7

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

8

Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation.

Ogata T, Wakui K, Kosho T, Muroya K, Yamanouchi Y, Takano T, Fukushima Y, Rappold G, Suzuki Y. Ogata T, et al. Am J Med Genet. 2000 Jun 5;92(4):256-9. Am J Med Genet. 2000. PMID: 10842291

9

Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.

Ogata T, Kosho T, Wakui K, Fukushima Y, Yoshimoto M, Miharu N. Ogata T, et al. J Clin Endocrinol Metab. 2000 Aug;85(8):2927-30. doi: 10.1210/jcem.85.8.6745. J Clin Endocrinol Metab. 2000. PMID: 10946905

10

Sex-determining gene(s) on distal 9p: clinical and molecular studies in six cases.

Muroya K, Okuyama T, Goishi K, Ogiso Y, Fukuda S, Kameyama J, Sato H, Suzuki Y, Terasaki H, Gomyo H, Wakui K, Fukushima Y, Ogata T. Muroya K, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2000 Sep;85(9):3094-100. doi: 10.1210/jcem.85.9.6771. J Clin Endocrinol Metab. 2000. PMID: 10999792 Clinical Trial.

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