Fukushima Y - Search Results

1

Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.

Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N. Kubota T, et al. Among authors: fukushima y. Am J Med Genet. 1994 Feb 15;49(4):378-83. doi: 10.1002/ajmg.1320490405. Am J Med Genet. 1994. PMID: 7909196

2

Molecular and clinical study of 61 Angelman syndrome patients.

Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, et al. Saitoh S, et al. Among authors: fukushima y. Am J Med Genet. 1994 Aug 15;52(2):158-63. doi: 10.1002/ajmg.1320520207. Am J Med Genet. 1994. PMID: 7802001 Review.

3

The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.

Ohta T, Tohma T, Soejima H, Fukushima Y, Nagai T, Yoshiura K, Jinno Y, Niikawa N. Ohta T, et al. Among authors: fukushima y. Hum Genet. 1993 Aug;92(1):1-5. doi: 10.1007/BF00216136. Hum Genet. 1993. PMID: 8365720

4

Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1.

Miyoshi O, Yabe R, Wakui K, Fukushima Y, Koizumi S, Uchikawa M, Kajii T, Numakura C, Takahashi S, Hayasaka K, Niikawa N. Miyoshi O, et al. Among authors: fukushima y. Am J Med Genet. 2001 Dec 1;104(3):250-6. Am J Med Genet. 2001. PMID: 11754053

5

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

6

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

7

A stable acentric marker chromosome: possible existence of an intercalary ancient centromere at distal 8p.

Ohashi H, Wakui K, Ogawa K, Okano T, Niikawa N, Fukushima Y. Ohashi H, et al. Among authors: fukushima y. Am J Hum Genet. 1994 Dec;55(6):1202-8. Am J Hum Genet. 1994. PMID: 7977381 Free PMC article.

8

Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.

Fukushima Y, Hoovers J, Mannens M, Wakui K, Ohashi H, Ohno T, Ueoka Y, Niikawa N. Fukushima Y, et al. Hum Genet. 1993 Apr;91(3):205-9. doi: 10.1007/BF00218257. Hum Genet. 1993. PMID: 8478003

9

Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.

Coêlho KE, Egashira M, Kato R, Fujimoto M, Matsumoto N, Rerkamnuaychoke B, Abe K, Harada N, Ohashi H, Fukushima Y, Niikawa N. Coêlho KE, et al. Among authors: fukushima y. Am J Med Genet. 1996 Jun 14;63(3):468-71. doi: 10.1002/(SICI)1096-8628(19960614)63:3<468::AID-AJMG10>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8737654

10

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.

Hatada I, Inazawa J, Abe T, Nakayama M, Kaneko Y, Jinno Y, Niikawa N, Ohashi H, Fukushima Y, Iida K, Yutani C, Takahashi S, Chiba Y, Ohishi S, Mukai T. Hatada I, et al. Among authors: fukushima y. Hum Mol Genet. 1996 Jun;5(6):783-8. doi: 10.1093/hmg/5.6.783. Hum Mol Genet. 1996. PMID: 8776593

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