Kurosawa K - Search Results

1

Screening for partial deletions in the CREBBP gene in Rubinstein-Taybi syndrome patients using multiplex PCR/liquid chromatography.

Udaka T, Kurosawa K, Izumi K, Yoshida S, Tsukahara M, Okamoto N, Torii C, Kosaki R, Masuno M, Hosokai N, Takahashi T, Kosaki K. Udaka T, et al. Among authors: kurosawa k. Genet Test. 2006 Winter;10(4):265-71. doi: 10.1089/gte.2006.10.265. Genet Test. 2006. PMID: 17253932

2

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

3

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

4

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

5

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.

6

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

7

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.

8

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.

9

A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy.

Okamoto N, Toribe Y, Nakajima T, Okinaga T, Kurosawa K, Nonaka I, Shimokawa O, Matsumoto N. Okamoto N, et al. Among authors: kurosawa k. J Hum Genet. 2002;47(10):556-9. doi: 10.1007/s100380200085. J Hum Genet. 2002. PMID: 12376748

10

Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome.

Miyake N, Kurotaki N, Sugawara H, Shimokawa O, Harada N, Kondoh T, Tsukahara M, Ishikiriyama S, Sonoda T, Miyoshi Y, Sakazume S, Fukushima Y, Ohashi H, Nagai T, Kawame H, Kurosawa K, Touyama M, Shiihara T, Okamoto N, Nishimoto J, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N. Miyake N, et al. Among authors: kurosawa k. Am J Hum Genet. 2003 May;72(5):1331-7. doi: 10.1086/375166. Epub 2003 Apr 9. Am J Hum Genet. 2003. PMID: 12687502 Free PMC article.

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