Ohama K - Search Results

1

Detection of chromosomal abnormalities of chromosome 12 in uterine leiomyoma using fluorescence in situ hybridization.

Hayashi S, Miharu N, Okamoto E, Samura O, Hara T, Ohama K. Hayashi S, et al. Among authors: ohama k. Jpn J Hum Genet. 1996 Mar;41(1):193-202. doi: 10.1007/BF01892627. Jpn J Hum Genet. 1996. PMID: 8914635

2

Chromosomal FISH analysis of unfertilized human oocytes and polar bodies.

Honda N, Miharu N, Hara T, Samura O, Honda H, Ohama K. Honda N, et al. Among authors: ohama k. J Hum Genet. 2002;47(9):488-91. doi: 10.1007/s100380200071. J Hum Genet. 2002. PMID: 12202989

3

Detection of chromosomal abnormalities in uterine leiomyoma using conventional cytogenetic method and interphase fluorescence in situ hybridization.

Hayashi S, Miharu N, Okamoto E, Samura O, Hara T, Ohama K. Hayashi S, et al. Among authors: ohama k. Cancer Genet Cytogenet. 1996 Jul 15;89(2):98-104. doi: 10.1016/0165-4608(95)00354-1. Cancer Genet Cytogenet. 1996. PMID: 8697434

4

[A case of giant uterine leiomyoma with chromosomal aberration].

Samura O, Hayashi S, Miharu N, Hara T, Ohama K, Matsubayashi S. Samura O, et al. Among authors: ohama k. Nihon Sanka Fujinka Gakkai Zasshi. 1996 Feb;48(2):149-52. Nihon Sanka Fujinka Gakkai Zasshi. 1996. PMID: 8718552 Japanese. No abstract available.

5

Detection of aneuploidy in human spermatozoa using fluorescence in situ hybridization (FISH).

Hu H, Miharu N, Mizunoe T, Nakaoka Y, Okamoto E, Ohama K. Hu H, et al. Among authors: ohama k. Jpn J Hum Genet. 1996 Dec;41(4):381-9. doi: 10.1007/BF01876328. Jpn J Hum Genet. 1996. PMID: 9088108

6

A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism.

Hayashi S, Miharu N, He H, Honda H, Samura O, Nakaoka Y, Ohama K. Hayashi S, et al. Among authors: ohama k. J Obstet Gynaecol Res. 1997 Jun;23(3):301-5. doi: 10.1111/j.1447-0756.1997.tb00849.x. J Obstet Gynaecol Res. 1997. PMID: 9255046

7

Chromosome analysis in human oocytes remaining unfertilized after in-vitro insemination: effect of maternal age and fertilization rate.

Nakaoka Y, Okamoto E, Miharu N, Ohama K. Nakaoka Y, et al. Among authors: ohama k. Hum Reprod. 1998 Feb;13(2):419-24. doi: 10.1093/humrep/13.2.419. Hum Reprod. 1998. PMID: 9557850

8

Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9)(q26.2;q32) and t(3;9)(p25;q32), by triple-color fluorescence in situ hybridization.

Honda H, Miharu N, Ohashi Y, Honda N, Hara T, Ohama K. Honda H, et al. Among authors: ohama k. Hum Genet. 1999 Nov;105(5):428-36. doi: 10.1007/s004390051126. Hum Genet. 1999. PMID: 10598808

9

Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization.

Honda H, Miharu N, Samura O, He H, Ohama K. Honda H, et al. Among authors: ohama k. Hum Genet. 2000 Feb;106(2):188-93. doi: 10.1007/s004390051027. Hum Genet. 2000. PMID: 10746560

10

High frequency of XY disomy in spermatozoa of severe oligozoospermic men.

Ohashi Y, Miharu N, Honda H, Samura O, Ohama K. Ohashi Y, et al. Among authors: ohama k. Hum Reprod. 2001 Apr;16(4):703-8. doi: 10.1093/humrep/16.4.703. Hum Reprod. 2001. PMID: 11278222 Free article.

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