Fukushima Y - Search Results

1

Interstitial duplication 8q22-q24: report of a case proven by FISH with mapped cosmid probes.

Wakui K, Ohashi H, Yamagishi A, Hamano S, Nara T, Ishikiriyama S, Nakamura Y, Fukushima Y. Wakui K, et al. Among authors: fukushima y. Am J Med Genet. 1996 Oct 2;65(1):36-9. doi: 10.1002/(SICI)1096-8628(19961002)65:1<36::AID-AJMG5>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8914738 Review.

2

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.

3

New diagnostic method for Pallister-Killian syndrome: detection of i(12p) in interphase nuclei of buccal mucosa by fluorescence in situ hybridization.

Ohashi H, Ishikiriyama S, Fukushima Y. Ohashi H, et al. Among authors: fukushima y. Am J Med Genet. 1993 Jan 1;45(1):123-8. doi: 10.1002/ajmg.1320450136. Am J Med Genet. 1993. PMID: 8418650

4

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

5

Tetramelic mirror-image polydactyly and a de novo balanced translocation between 2p23.3 and 14q13.

Kim KC, Wakui K, Yamagishi A, Ohno T, Sato M, Imaizumi S, Aihara T, Fukushima Y, Ohashi H. Kim KC, et al. Among authors: fukushima y. Am J Med Genet. 1997 Jan 10;68(1):70-3. doi: 10.1002/(sici)1096-8628(19970110)68:1<70::aid-ajmg13>3.0.co;2-l. Am J Med Genet. 1997. PMID: 8986279

6

Pseudoachondroplasia with de novo deletion [del(11)(q21q22.2)].

Ikegawa S, Ohashi H, Hosoda F, Fukushima Y, Ohki M, Nakamura Y. Ikegawa S, et al. Among authors: fukushima y. Am J Med Genet. 1998 Jun 5;77(5):356-9. doi: 10.1002/(sici)1096-8628(19980605)77:5<356::aid-ajmg3>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9632164

7

Blepharophimosis sequence and de novo balanced autosomal translocation [46,XY,t(3;4)(q23;p15.2)]: possible assignment of the trait to 3q23.

Fukushima Y, Wakui K, Nishida T, Ueoka Y. Fukushima Y, et al. Am J Med Genet. 1991 Sep 15;40(4):485-7. doi: 10.1002/ajmg.1320400423. Am J Med Genet. 1991. PMID: 1746616

8

Craniosynostosis in an infant with an interstitial deletion of 15q [46,XY,del(15)(q15q22.1)].

Fukushima Y, Wakui K, Nishida T, Nishimoto H. Fukushima Y, et al. Am J Med Genet. 1990 Jun;36(2):209-13. doi: 10.1002/ajmg.1320360214. Am J Med Genet. 1990. PMID: 2368808

9

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

10

Precise chromosomal locations of the genes for dentatorubral-pallidoluysian atrophy (DRPLA), von Willebrand factor (F8vWF) and parathyroid hormone-like hormone (PTHLH) in human chromosome 12p by deletion mapping.

Kuwano A, Morimoto Y, Nagai T, Fukushima Y, Ohashi H, Hasegawa T, Kondo I. Kuwano A, et al. Among authors: fukushima y. Hum Genet. 1996 Jan;97(1):95-8. doi: 10.1007/BF00218841. Hum Genet. 1996. PMID: 8557270

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

1,669 results

Search Page

Filters