Okamura K - Search Results

1

Complete XY gonadal dysgenesis and aspects of the SRYgenotype and gonadal tumor formation.

Uehara S, Hashiyada M, Sato K, Nata M, Funato T, Okamura K. Uehara S, et al. Among authors: okamura k. J Hum Genet. 2002;47(6):279-84. doi: 10.1007/s100380200040. J Hum Genet. 2002. PMID: 12111377

2

X-chromosome inactivation in the human trophoblast of early pregnancy.

Uehara S, Tamura M, Nata M, Ji G, Yaegashi N, Okamura K, Yajima A. Uehara S, et al. Among authors: okamura k. J Hum Genet. 2000;45(3):119-26. doi: 10.1007/s100380050197. J Hum Genet. 2000. PMID: 10807535

3

X chromosome inactivation patterns in 45,X/46,XX mosaics.

Uehara S, Sato K, Hashiyada M, Obara Y, Matsuzaki S, Nata M, Okamura K. Uehara S, et al. Among authors: okamura k. J Hum Genet. 2001;46(3):126-31. doi: 10.1007/s100380170099. J Hum Genet. 2001. PMID: 11310579

4

Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss.

Uehara S, Hashiyada M, Sato K, Sato Y, Fujimori K, Okamura K. Uehara S, et al. Among authors: okamura k. Fertil Steril. 2001 Nov;76(5):908-14. doi: 10.1016/s0015-0282(01)02845-x. Fertil Steril. 2001. PMID: 11704109 Free article.

5

Paracentric inversion of chromosome 14: a case report.

Uehara S, Tanigawara S, Takeyama Y, Takabayashi T, Okamura K, Yajima A. Uehara S, et al. Among authors: okamura k. Jpn J Hum Genet. 1994 Sep;39(3):353-6. doi: 10.1007/BF01874054. Jpn J Hum Genet. 1994. PMID: 7841446

6

A family with pericentric inversion of chromosome 12.

Uehara S, Tanigawara S, Takeyama Y, Okamura K, Yajima A. Uehara S, et al. Among authors: okamura k. Jpn J Hum Genet. 1994 Mar;39(1):201-4. doi: 10.1007/BF01915957. Jpn J Hum Genet. 1994. PMID: 8025298

7

Familial pericentric inversion incidentally detected at prenatal diagnosis.

Uehara S, Takabayashi T, Takeyama Y, Okamura K, Yajima A. Uehara S, et al. Among authors: okamura k. Jpn J Hum Genet. 1995 Sep;40(3):259-63. doi: 10.1007/BF01876184. Jpn J Hum Genet. 1995. PMID: 8527800

8

Compound heterozygous mutations (PHE53/54DEL and HIS373LEU) of the P450c17 gene result in a 17alpha-hydroxylase/17,20-lyase deficient male pseudohermaphrodite with unambiguous external genitalia.

Uehara S, Sato J, Nishiyama Y, Matsuzaki S, Funato T, Murotsuki J, Yaegashi N, Okamura K, Yajima A. Uehara S, et al. Among authors: okamura k. Tohoku J Exp Med. 2000 Apr;190(4):279-87. doi: 10.1620/tjem.190.279. Tohoku J Exp Med. 2000. PMID: 10877510 Free article.

9

Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature.

Uehara S, Hanew K, Harada N, Yamamori S, Nata M, Niikawa N, Okamura K. Uehara S, et al. Among authors: okamura k. Am J Med Genet. 2001 Mar 15;99(3):196-9. doi: 10.1002/1096-8628(20010315)99:3<196::aid-ajmg1157>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11241489

10

Molecular biologic analyses of tetragametic chimerism in a true hermaphrodite with 46,XX/46,XY.

Uehara S, Nata M, Nagae M, Sagisaka K, Okamura K, Yajima A. Uehara S, et al. Among authors: okamura k. Fertil Steril. 1995 Jan;63(1):189-92. doi: 10.1016/s0015-0282(16)57317-8. Fertil Steril. 1995. PMID: 7805911 Free article.

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