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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 4
2003 1
2004 1
2005 2
2006 1
2007 2
2011 3
2012 2
2020 1
2021 1
2022 2
2024 1

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19 results

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Page 1
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.
Trends in occurrence of twin births in Japan.
Kurosawa K, Masuno M, Kuroki Y. Kurosawa K, et al. Among authors: kuroki y. Am J Med Genet A. 2012 Jan;158A(1):75-7. doi: 10.1002/ajmg.a.34362. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22106070
Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome.
Murakami H, Tsurusaki Y, Enomoto K, Kuroda Y, Yokoi T, Furuya N, Yoshihashi H, Minatogawa M, Abe-Hatano C, Ohashi I, Nishimura N, Kumaki T, Enomoto Y, Naruto T, Iwasaki F, Harada N, Ishikawa A, Kawame H, Sameshima K, Yamaguchi Y, Kobayashi M, Tominaga M, Ishikiriyama S, Tanaka T, Suzumura H, Ninomiya S, Kondo A, Kaname T, Kosaki K, Masuno M, Kuroki Y, Kurosawa K. Murakami H, et al. Among authors: kuroki y. Am J Med Genet A. 2020 Oct;182(10):2333-2344. doi: 10.1002/ajmg.a.61793. Epub 2020 Aug 17. Am J Med Genet A. 2020. PMID: 32803813
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
Ehlers-Danlos syndrome, vascular type: a novel missense mutation in the COL3A1 gene.
Masuno M, Watanabe A, Naing BT, Shimada T, Fujimoto W, Ninomiya S, Ueda Y, Kadota K, Kotaka T, Kondo E, Yamanouchi Y, Inoue M, Ouchi K, Kuroki Y. Masuno M, et al. Among authors: kuroki y. Congenit Anom (Kyoto). 2012 Dec;52(4):207-10. doi: 10.1111/j.1741-4520.2011.00353.x. Congenit Anom (Kyoto). 2012. PMID: 23181496
19 results