Imaizumi K - Search Results

1

Congenital heart defect in a patient with the Hallermann-Streiff syndrome.

Imaizumi K, Makita Y, Masuno M, Kuroki Y. Imaizumi K, et al. Am J Med Genet. 1994 Dec 1;53(4):386-7. doi: 10.1002/ajmg.1320530419. Am J Med Genet. 1994. PMID: 7864053 No abstract available.

2

Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism, and mental retardation.

Imaizumi K, Kuroki Y. Imaizumi K, et al. Am J Med Genet. 1991 Nov 1;41(2):162-3. doi: 10.1002/ajmg.1320410204. Am J Med Genet. 1991. PMID: 1785626 No abstract available.

3

Rubinstein-Taybi syndrome with de novo reciprocal translocation t(2;16)(p13.3;p13.3).

Imaizumi K, Kuroki Y. Imaizumi K, et al. Am J Med Genet. 1991 Mar 15;38(4):636-9. doi: 10.1002/ajmg.1320380430. Am J Med Genet. 1991. PMID: 2063911

4

Rieger syndrome with de novo reciprocal translocation t(1;4) (q23.1;q25).

Makita Y, Masuno M, Imaizumi K, Yamashita S, Ohba S, Ito D, Kuroki Y. Makita Y, et al. Among authors: imaizumi k. Am J Med Genet. 1995 May 22;57(1):19-21. doi: 10.1002/ajmg.1320570106. Am J Med Genet. 1995. PMID: 7645592 Review.

5

Autosomal dominant inheritance in Setleis syndrome.

Masuno M, Imaizumi K, Makita Y, Nakamura M, Kuroki Y. Masuno M, et al. Among authors: imaizumi k. Am J Med Genet. 1995 May 22;57(1):57-60. doi: 10.1002/ajmg.1320570113. Am J Med Genet. 1995. PMID: 7645599

6

Submicroscopic deletion of chromosome region 16p13.3 in a Japanese patient with Rubinstein-Taybi syndrome.

Masuno M, Imaizumi K, Kurosawa K, Makita Y, Petrij F, Dauwerse HG, Breuning MH, Kuroki Y. Masuno M, et al. Among authors: imaizumi k. Am J Med Genet. 1994 Dec 1;53(4):352-4. doi: 10.1002/ajmg.1320530409. Am J Med Genet. 1994. PMID: 7864045

7

Epidemiology of limb-body wall complex in Japan.

Kurosawa K, Imaizumi K, Masuno M, Kuroki Y. Kurosawa K, et al. Among authors: imaizumi k. Am J Med Genet. 1994 Jun 1;51(2):143-6. doi: 10.1002/ajmg.1320510212. Am J Med Genet. 1994. PMID: 8092190

8

Hypoglycemia in Coffin-Siris syndrome.

Imaizumi K, Nakamura M, Masuno M, Makita Y, Kuroki Y. Imaizumi K, et al. Am J Med Genet. 1995 Oct 23;59(1):49-50. doi: 10.1002/ajmg.1320590111. Am J Med Genet. 1995. PMID: 8849011

9

SPONASTRIME dysplasia: report on a female patient with severe skeletal changes.

Masuno M, Nishimura G, Adachi M, Hotsubo T, Tachibana K, Makita Y, Imaizumi K, Kuroki Y. Masuno M, et al. Among authors: imaizumi k. Am J Med Genet. 1996 Dec 30;66(4):429-32. doi: 10.1002/(SICI)1096-8628(19961230)66:4<429::AID-AJMG8>3.0.CO;2-F. Am J Med Genet. 1996. PMID: 8989461

10

Magnetic resonance imaging abnormalities of the brain in Goldberg-Shprintzen syndrome (Hirschsprung disease, microcephaly, and iris coloboma).

Ohnuma K, Imaizumi K, Masuno M, Nakamura M, Kuroki Y. Ohnuma K, et al. Among authors: imaizumi k. Am J Med Genet. 1997 Dec 12;73(2):230-2. Am J Med Genet. 1997. PMID: 9409878 No abstract available.

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