Kurosawa K - Search Results

1

Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl.

Enomoto K, Kishitani Y, Tominaga M, Ishikawa A, Furuya N, Aida N, Masuno M, Yamada K, Kurosawa K. Enomoto K, et al. Among authors: kurosawa k. Am J Med Genet A. 2012 Sep;158A(9):2347-52. doi: 10.1002/ajmg.a.35542. Epub 2012 Aug 7. Am J Med Genet A. 2012. PMID: 22887762

2

Osteodysplastic primordial dwarfism: a case with features of type II.

Masuno M, Imaizumi K, Nishimura G, Kurosawa K, Makita Y, Shimazaki Y, Kuroki Y. Masuno M, et al. Among authors: kurosawa k. Clin Dysmorphol. 1995 Jan;4(1):57-62. Clin Dysmorphol. 1995. PMID: 7735506 Review.

3

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: kurosawa k. Am J Med Genet. 1994 Dec 1;53(4):352-4. doi: 10.1002/ajmg.1320530409. Am J Med Genet. 1994. PMID: 7864045

4

Epidemiology of limb-body wall complex in Japan.

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

5

Male with type II autosomal recessive cutis laxa.

Imaizumi K, Kurosawa K, Makita Y, Masuno M, Kuroki Y. Imaizumi K, et al. Among authors: kurosawa k. Clin Genet. 1994 Jan;45(1):40-3. doi: 10.1111/j.1399-0004.1994.tb03988.x. Clin Genet. 1994. PMID: 8149651

6

Chromosome aberrations in Rubinstein-Taybi syndrome.

Imaizumi K, Kurosawa K, Masuno M, Tsukahara M, Kuroki Y. Imaizumi K, et al. Among authors: kurosawa k. Clin Genet. 1993 Apr;43(4):215-6. doi: 10.1111/j.1399-0004.1993.tb04468.x. Clin Genet. 1993. PMID: 8330456 No abstract available.

7

Sotos syndrome associated with a de novo balanced reciprocal translocation t(5;8)(q35;q24.1).

Imaizumi K, Kimura J, Matsuo M, Kurosawa K, Masuno M, Niikawa N, Kuroki Y. Imaizumi K, et al. Among authors: kurosawa k. Am J Med Genet. 2002 Jan 1;107(1):58-60. doi: 10.1002/ajmg.10080. Am J Med Genet. 2002. PMID: 11807869

8

Premature thelarche in Rubinstein-Taybi syndrome.

Kurosawa K, Masuno M, Imaizumi K, Matsuo M, Kuroki Y, Tachibana K. Kurosawa K, et al. Am J Med Genet. 2002 Apr 15;109(1):72-3. doi: 10.1002/ajmg.10297. Am J Med Genet. 2002. PMID: 11932997 Review. No abstract available.

9

Gonadal sex cord stromal tumor in a patient with Rubinstein-Taybi syndrome.

Kurosawa K, Fukutani K, Masuno M, Kawame H, Ochiai Y. Kurosawa K, et al. Pediatr Int. 2002 Jun;44(3):330-2. doi: 10.1046/j.1442-200x.2002.01539.x. Pediatr Int. 2002. PMID: 11982910 No abstract available.

10

Paternal UPD14 is responsible for a distinctive malformation complex.

Kurosawa K, Sasaki H, Sato Y, Yamanaka M, Shimizu M, Ito Y, Okuyama T, Matsuo M, Imaizumi K, Kuroki Y, Nishimura G. Kurosawa K, et al. Am J Med Genet. 2002 Jul 1;110(3):268-72. doi: 10.1002/ajmg.10404. Am J Med Genet. 2002. PMID: 12116236

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