Maeda T - Search Results

1

Postzygotic D/D translocation homozygosity associated with recurrent abortions.

Maeda T, Ohno M, Takada M, Matsunobu A, Arai M. Maeda T, et al. Am J Med Genet. 1983 Jul;15(3):389-92. doi: 10.1002/ajmg.1320150304. Am J Med Genet. 1983. PMID: 6881208

2

A 22/22 translocation carrier with recurrent abortions demonstrated by a Giemsa banding technique,

Maeda T, Ohno M, Shimada N, Nishida M, Jobo T. Maeda T, et al. Hum Genet. 1976 Feb 29;31(2):243-5. doi: 10.1007/BF00296154. Hum Genet. 1976. PMID: 1248834

3

[Cytogenetic studies in couples with repeated spontaneous abortions].

Ohno M, Maeda T, Funato T, Yabe N, Matsunobu A, Yoshihara K. Ohno M, et al. Among authors: maeda t. Nihon Sanka Fujinka Gakkai Zasshi. 1989 Sep;41(9):1387-93. Nihon Sanka Fujinka Gakkai Zasshi. 1989. PMID: 2584818 Japanese.

4

Turner's syndrome with a duplication-deficiency X chromosome derived from a maternal pericentric inversion X chromosome.

Maeda T, Ohno M, Takada M, Nishida M, Tsukioka K, Tomita H. Maeda T, et al. Clin Genet. 1979 Mar;15(3):259-66. doi: 10.1111/j.1399-0004.1979.tb00977.x. Clin Genet. 1979. PMID: 421365

5

Clinical and cytogenetic studies of two infants with partial monosomy G.

Maeda T, Ohno M, Nishida H. Maeda T, et al. Hum Genet. 1977 Mar 14;35(3):255-9. doi: 10.1007/BF00446618. Hum Genet. 1977. PMID: 844874

6

A cytogenetic study of spontaneous abortions with direct analysis of chorionic villi.

Ohno M, Maeda T, Matsunobu A. Ohno M, et al. Among authors: maeda t. Obstet Gynecol. 1991 Mar;77(3):394-8. Obstet Gynecol. 1991. PMID: 1992406 Review.

7

A cytogenetic survey of 14,835 consecutive liveborns.

Maeda T, Ohno M, Matsunobu A, Yoshihara K, Yabe N. Maeda T, et al. Jinrui Idengaku Zasshi. 1991 Mar;36(1):117-29. doi: 10.1007/BF01876812. Jinrui Idengaku Zasshi. 1991. PMID: 2062008

8

Monozygotic twins of different apparent sex.

Yokota Y, Akane A, Fujino N, Sato Y, Matsunobu A, Matsuura N, Maeda T, Tadokoro M, Nakahori Y, Nakagome Y. Yokota Y, et al. Among authors: maeda t. Am J Med Genet. 1994 Oct 15;53(1):52-5. doi: 10.1002/ajmg.1320530111. Am J Med Genet. 1994. PMID: 7802036

9

A cytogenetic survey of consecutive liveborn infants-incidence and type of chromosome abnormalities.

Maeda T, Ohno M, Takada M, Kato Y, Nishida M, Jobo T, Adachi H, Taguchi A. Maeda T, et al. Jinrui Idengaku Zasshi. 1978 Sep;23(3):217-24. doi: 10.1007/BF01872471. Jinrui Idengaku Zasshi. 1978. PMID: 732017 No abstract available.

10

Ring Y chromosome: 45,X/46,Xr(Y) chromosome mosaicism in a phenotypically normal male with azoospermia.

Maeda T, Ohno M, Ishibashi A, Samejima M, Sasaki K. Maeda T, et al. Hum Genet. 1976 Sep 10;34(1):99-102. doi: 10.1007/BF00284445. Hum Genet. 1976. PMID: 965013 No abstract available.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

5,640 results

Search Page

Filters