Kuroki Y - Search Results

1

Metacarpophalangeal pattern profile analysis in 14 Japanese children with Sotos syndrome.

Takahashi Y, Imaizumi K, Takada F, Kuroki Y. Takahashi Y, et al. Among authors: kuroki y. Jpn J Hum Genet. 1994 Mar;39(1):187-91. doi: 10.1007/BF01915954. Jpn J Hum Genet. 1994. PMID: 8025295

2

Asphyxiating thoracic dystrophy: surgical correction and 2-year follow-up in a girl.

Takada F, Hiroki K, Ohkawa Y, Imaizumi K, Kuroki Y. Takada F, et al. Among authors: kuroki y. Jpn J Hum Genet. 1994 Jun;39(2):269-73. doi: 10.1007/BF01876848. Jpn J Hum Genet. 1994. PMID: 8086645

3

Epidemiology of limb-body wall complex in Japan.

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

4

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

Imaizumi K, Kuroki Y. Imaizumi K, et al. Among authors: kuroki y. 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.

5

Cytogenetic and molecular study of Angelman syndrome.

Imaizumi K, Takada F, Kuroki Y, Naritomi K, Hamabe J, Niikawa N. Imaizumi K, et al. Among authors: kuroki y. Am J Med Genet. 1990 Mar;35(3):314-8. doi: 10.1002/ajmg.1320350305. Am J Med Genet. 1990. PMID: 2309778

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: kuroki y. Am J Med Genet. 2002 Jan 1;107(1):58-60. doi: 10.1002/ajmg.10080. Am J Med Genet. 2002. PMID: 11807869

7

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: kuroki y. Am J Med Genet. 1995 May 22;57(1):19-21. doi: 10.1002/ajmg.1320570106. Am J Med Genet. 1995. PMID: 7645592 Review.

8

Autosomal dominant inheritance in Setleis syndrome.

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

9

Molecular and clinical study of 61 Angelman syndrome patients.

Saitoh S, Harada N, Jinno Y, Hashimoto K, Imaizumi K, Kuroki Y, Fukushima Y, Sugimoto T, Renedo M, Wagstaff J, et al. Saitoh S, et al. Among authors: kuroki y. Am J Med Genet. 1994 Aug 15;52(2):158-63. doi: 10.1002/ajmg.1320520207. Am J Med Genet. 1994. PMID: 7802001 Review.

10

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

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