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Premature thelarche in Rubinstein-Taybi syndrome.
Kurosawa K, Masuno M, Imaizumi K, Matsuo M, Kuroki Y, Tachibana K. Kurosawa K, et al. Among authors: kuroki y. 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.
Pilomatrixomas in Rubinstein-Taybi syndrome.
Masuno M, Imaizumi K, Ishii T, Kuroki Y, Baba N, Tanaka Y. Masuno M, et al. Among authors: kuroki y. Am J Med Genet. 1998 Apr 28;77(1):81-2. doi: 10.1002/(sici)1096-8628(19980428)77:1<81::aid-ajmg19>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9557902 No abstract available.
Chromosome aberrations in Rubinstein-Taybi syndrome.
Imaizumi K, Kurosawa K, Masuno M, Tsukahara M, Kuroki Y. Imaizumi K, et al. Among authors: kuroki y. 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.
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. Among authors: kuroki y. Am J Med Genet. 2002 Jul 1;110(3):268-72. doi: 10.1002/ajmg.10404. Am J Med Genet. 2002. PMID: 12116236
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
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
725 results