Fukushima Y - Search Results

1

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

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

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.

4

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

5

HDR syndrome (hypoparathyroidism, sensorineural deafness, renal dysplasia) associated with del(10)(p13).

Hasegawa T, Hasegawa Y, Aso T, Koto S, Nagai T, Tsuchiya Y, Kim KC, Ohashi H, Wakui K, Fukushima Y. Hasegawa T, et al. Among authors: fukushima y. Am J Med Genet. 1997 Dec 31;73(4):416-8. doi: 10.1002/(sici)1096-8628(19971231)73:4<416::aid-ajmg9>3.0.co;2-l. Am J Med Genet. 1997. PMID: 9415468 Review.

6

4q33-qter deletion and absorptive hypercalciuria: report of two unrelated girls.

Imamura K, Tonoki H, Wakui K, Fukushima Y, Sasaki S, Yausda K, Takekoshi Y, Tochimaru H. Imamura K, et al. Among authors: fukushima y. Am J Med Genet. 1998 Jun 16;78(1):52-4. Am J Med Genet. 1998. PMID: 9637423

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

De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2-4q31.1.

Wakui K, Nishida T, Masuda J, Itoh T, Katsumata D, Ohno T, Fukushima Y. Wakui K, et al. Among authors: fukushima y. Jinrui Idengaku Zasshi. 1991 Jun;36(2):149-53. doi: 10.1007/BF01876577. Jinrui Idengaku Zasshi. 1991. PMID: 1920913

9

Specification of small distal 6q deletions in two patients by gene dosage and in situ hybridization study of plasminogen and alpha-L-fucosidase 2.

Narahara K, Tsuji K, Yokoyama Y, Namba H, Murakami M, Matsubara T, Kasai R, Fukushima Y, Seki T, Wakui K, et al. Narahara K, et al. Among authors: fukushima y. Am J Med Genet. 1991 Sep 1;40(3):348-53. doi: 10.1002/ajmg.1320400322. Am J Med Genet. 1991. PMID: 1951444

10

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

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