Fukushima Y - Search Results

1

De novo apparently balanced reciprocal translocation between 5q11.2 and 17q23 associated with Klippel-Feil anomaly and type A1 brachydactyly.

Fukushima Y, Ohashi H, Wakui K, Nishimoto H, Sato M, Aihara T. Fukushima Y, et al. Am J Med Genet. 1995 Jul 3;57(3):447-9. doi: 10.1002/ajmg.1320570317. Am J Med Genet. 1995. PMID: 7677149

2

Deletion of the KIT and PDGFRA genes in a patient with piebaldism.

Spritz RA, Droetto S, Fukushima Y. Spritz RA, et al. Among authors: fukushima y. Am J Med Genet. 1992 Nov 1;44(4):492-5. doi: 10.1002/ajmg.1320440422. Am J Med Genet. 1992. PMID: 1279971

3

Cloning and characterization of the inversion breakpoint at chromosome 2q35 in a patient with Waardenburg syndrome type I.

Tsukamoto K, Tohma T, Ohta T, Yamakawa K, Fukushima Y, Nakamura Y, Niikawa N. Tsukamoto K, et al. Among authors: fukushima y. Hum Mol Genet. 1992 Aug;1(5):315-7. doi: 10.1093/hmg/1.5.315. Hum Mol Genet. 1992. PMID: 1303207

4

A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell lines.

Fukushima Y, Ohashi H, Wakui K, Nishida T, Oh-ishi T. Fukushima Y, et al. Jpn J Hum Genet. 1992 Jun;37(2):149-50. doi: 10.1007/BF01899737. Jpn J Hum Genet. 1992. PMID: 1327290

5

DNA analyses of XX and XX-hypospadiac males.

Numabe H, Nagafuchi S, Nakahori Y, Tamura T, Kiuchi H, Namiki M, Kohda N, Fukushima Y, Fuse H, Kusano M, et al. Numabe H, et al. Among authors: fukushima y. Hum Genet. 1992 Nov;90(3):211-4. doi: 10.1007/BF00220064. Hum Genet. 1992. PMID: 1487232

6

Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?

Naritomi K, Izumikawa Y, Nagataki S, Fukushima Y, Wakui K, Niikawa N, Hirayama K. Naritomi K, et al. Among authors: fukushima y. Am J Med Genet. 1992 Jul 15;43(5):839-43. doi: 10.1002/ajmg.1320430517. Am J Med Genet. 1992. PMID: 1642272

7

Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs.

Deng HX, Abe K, Kondo I, Tsukahara M, Inagaki H, Hamada I, Fukushima Y, Niikawa N. Deng HX, et al. Among authors: fukushima y. Hum Genet. 1991 Apr;86(6):541-4. doi: 10.1007/BF00201538. Hum Genet. 1991. PMID: 1673956

8

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2.

Niikawa N, Deng HX, Abe K, Harada N, Okada T, Tsuchiya H, Akaboshi I, Matsuda I, Fukushima Y, Kaneko Y, et al. Niikawa N, et al. Among authors: fukushima y. Hum Genet. 1991 Sep;87(5):561-6. doi: 10.1007/BF00209012. Hum Genet. 1991. PMID: 1680787

9

Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.

Hamabe J, Fukushima Y, Harada N, Abe K, Matsuo N, Nagai T, Yoshioka A, Tonoki H, Tsukino R, Niikawa N. Hamabe J, et al. Among authors: fukushima y. Am J Med Genet. 1991 Oct 1;41(1):54-63. doi: 10.1002/ajmg.1320410116. Am J Med Genet. 1991. PMID: 1683159

10

DNA deletion and its parental origin in Angelman syndrome patients.

Hamabe J, Kuroki Y, Imaizumi K, Sugimoto T, Fukushima Y, Yamaguchi A, Izumikawa Y, Niikawa N. Hamabe J, et al. Among authors: fukushima y. Am J Med Genet. 1991 Oct 1;41(1):64-8. doi: 10.1002/ajmg.1320410117. Am J Med Genet. 1991. PMID: 1683160

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