Hasegawa T - Search Results

1

MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration.

Hamanaka K, Takata A, Uchiyama Y, Miyatake S, Miyake N, Mitsuhashi S, Iwama K, Fujita A, Imagawa E, Alkanaq AN, Koshimizu E, Azuma Y, Nakashima M, Mizuguchi T, Saitsu H, Wada Y, Minami S, Katoh-Fukui Y, Masunaga Y, Fukami M, Hasegawa T, Ogata T, Matsumoto N. Hamanaka K, et al. Among authors: hasegawa t. Hum Mol Genet. 2019 Jul 15;28(14):2319-2329. doi: 10.1093/hmg/ddz066. Hum Mol Genet. 2019. PMID: 30985895

2

Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis.

Fujita H, Kosaki R, Yoshihashi H, Ogata T, Tomita M, Hasegawa T, Takahashi T, Matsuo N, Kosaki K. Fujita H, et al. Among authors: hasegawa t. Teratology. 2002 Jan;65(1):10-8. doi: 10.1002/tera.1093. Teratology. 2002. PMID: 11835227

3

Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development.

Sasaki G, Ogata T, Ishii T, Hasegawa T, Sato S, Matsuo N. Sasaki G, et al. Among authors: hasegawa t. Am J Med Genet. 2002 Jul 15;110(4):365-9. doi: 10.1002/ajmg.10447. Am J Med Genet. 2002. PMID: 12116211

4

PTPN11 (protein-tyrosine phosphatase, nonreceptor-type 11) mutations in seven Japanese patients with Noonan syndrome.

Kosaki K, Suzuki T, Muroya K, Hasegawa T, Sato S, Matsuo N, Kosaki R, Nagai T, Hasegawa Y, Ogata T. Kosaki K, et al. Among authors: hasegawa t, hasegawa y. J Clin Endocrinol Metab. 2002 Aug;87(8):3529-33. doi: 10.1210/jcem.87.8.8694. J Clin Endocrinol Metab. 2002. PMID: 12161469

5

Duplication of 8p23.2: a benign cytogenetic variant?

Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, Ida T, Yoshiura K, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N. Harada N, et al. Among authors: hasegawa t. Am J Med Genet. 2002 Aug 15;111(3):285-8. doi: 10.1002/ajmg.10584. Am J Med Genet. 2002. PMID: 12210324

6

Giant seminoma in a patient with 5 alpha-reductase type 2 deficiency.

Sasaki G, Nakagawa K, Hashiguchi A, Hasegawa T, Ogata T, Murai M. Sasaki G, et al. Among authors: hasegawa t. J Urol. 2003 Mar;169(3):1080-1. doi: 10.1097/01.ju.0000047621.66463.29. J Urol. 2003. PMID: 12576851 No abstract available.

7

Micropenis and the 5alpha-reductase-2 (SRD5A2) gene: mutation and V89L polymorphism analysis in 81 Japanese patients.

Sasaki G, Ogata T, Ishii T, Kosaki K, Sato S, Homma K, Takahashi T, Hasegawa T, Matsuo N. Sasaki G, et al. Among authors: hasegawa t. J Clin Endocrinol Metab. 2003 Jul;88(7):3431-6. doi: 10.1210/jc.2002-021415. J Clin Endocrinol Metab. 2003. PMID: 12843198

8

Mental retardation in a boy with congenital adrenal hypoplasia: a clue to contiguous gene syndrome involving DAX1 and IL1RAPL.

Sasaki R, Inamo Y, Saitoh K, Hasegawa T, Kinoshita E, Ogata T. Sasaki R, et al. Among authors: hasegawa t. Endocr J. 2003 Jun;50(3):303-7. doi: 10.1507/endocrj.50.303. Endocr J. 2003. PMID: 12940459 Free article.

9

Longitudinal auxological study in a female with SHOX (short stature homeobox containing gene) haploinsufficiency and normal ovarian function.

Fukami M, Matsuo N, Hasegawa T, Sato S, Ogata T. Fukami M, et al. Among authors: hasegawa t. Eur J Endocrinol. 2003 Oct;149(4):337-41. doi: 10.1530/eje.0.1490337. Eur J Endocrinol. 2003. PMID: 14514349

10

Premature ovarian failure in a female with proximal symphalangism and Noggin mutation.

Kosaki K, Sato S, Hasegawa T, Matsuo N, Suzuki T, Ogata T. Kosaki K, et al. Among authors: hasegawa t. Fertil Steril. 2004 Apr;81(4):1137-9. doi: 10.1016/j.fertnstert.2003.08.054. Fertil Steril. 2004. PMID: 15066478 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

6,326 results

Search Page