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Page 1
Chondrodysplasia punctata with X;Y translocation.
Agematsu K, Koike K, Morosawa H, Nakahori Y, Nakagome Y, Akabane T. Agematsu K, et al. Among authors: nakagome y. Hum Genet. 1988 Sep;80(1):105-7. doi: 10.1007/BF00451470. Hum Genet. 1988. PMID: 3417299
Localization of 24 cosmid clones on the human Y chromosome.
Nagafuchi S, Nakahori Y, Nakamura Y, England SB, Tamura T, Numabe H, Nakagome Y. Nagafuchi S, et al. Among authors: nakagome y. Jpn J Hum Genet. 1992 Dec;37(4):307-10. doi: 10.1007/BF01883322. Jpn J Hum Genet. 1992. PMID: 1297451
DNA analysis of two patients with a non-fluorescent Y chromosome.
Sekine T, Fukutani K, Motegi T, Hayakawa H, Tamura T, Nagafuchi S, Nakahori Y, Nakagome Y. Sekine T, et al. Among authors: nakagome y. Jpn J Hum Genet. 1992 Jun;37(2):157-62. doi: 10.1007/BF01899739. Jpn J Hum Genet. 1992. PMID: 1391971
PCR detection of structurally abnormal Y chromosomes.
Nagafuchi S, Seki S, Nakahori Y, Tamura T, Numabe H, Nakagome Y. Nagafuchi S, et al. Among authors: nakagome y. Jpn J Hum Genet. 1992 Sep;37(3):187-93. doi: 10.1007/BF01900712. Jpn J Hum Genet. 1992. PMID: 1472700
Partial trisomy of the distal segment 14q.
Nakamura Y, Sakai K, Sakuma S, Sato E, Maruyama M, Hashimoto T, Fukuda S, Nishimi Y, Nakagome Y, Nakahori Y, et al. Nakamura Y, et al. Among authors: nakagome y. Hum Genet. 1990 May;84(6):574-6. doi: 10.1007/BF00210813. Hum Genet. 1990. PMID: 2338344
11q trisomy detected by fluorescence in situ hybridization.
Takano T, Yamanouchi Y, Kawashima S, Date M, Hashira S, Kida M, Abe T, Nakahori Y, Nakagome Y. Takano T, et al. Among authors: nakagome y. Clin Genet. 1993 Dec;44(6):324-8. doi: 10.1111/j.1399-0004.1993.tb03909.x. Clin Genet. 1993. PMID: 8131305
168 results