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

Year Number of Results
1980 2
1984 1
1985 1
1987 1
1991 1
1996 1
1997 1
2000 2
2001 1
2004 2
2005 1
2023 0

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13 results

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Page 1
[Trisomy 13 syndrome, Patau syndrome].
Tsukino R, Sasaki M. Tsukino R, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):332-4. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057250 Review. Japanese. No abstract available.
[Monosomy 13q syndrome].
Tsukino R, Sasaki M. Tsukino R, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):329-31. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057249 Review. Japanese. No abstract available.
Familial occurrence of oligomeganephronia.
Kusuyama Y, Tsukino R, Oomori H, Kuribayashi K, Katayama H, Koike M, Saito K. Kusuyama Y, et al. Among authors: tsukino r. Acta Pathol Jpn. 1985 Mar;35(2):449-57. doi: 10.1111/j.1440-1827.1985.tb00587.x. Acta Pathol Jpn. 1985. PMID: 4024943
Ring chromosome 10:46,XX,r(10)(p15 leads to q26).
Tsukino R, Tsuda N, Dezawa T, Ishii T, Koike M. Tsukino R, et al. J Med Genet. 1980 Apr;17(2):148-50. doi: 10.1136/jmg.17.2.148. J Med Genet. 1980. PMID: 7381872 Free PMC article.
1p36 deletion syndrome with intestinal malrotation and annular pancreas.
Minami K, Boshi H, Minami T, Tamura A, Yanagawa T, Uemura S, Takifuji K, Kurosawa K, Tsukino R, Izumi G, Yoshikawa N. Minami K, et al. Among authors: tsukino r. Eur J Pediatr. 2005 Mar;164(3):193-4. doi: 10.1007/s00431-004-1581-z. Epub 2004 Nov 17. Eur J Pediatr. 2005. PMID: 15717182 No abstract available.
Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation.
Harada N, Hatchwell E, Okamoto N, Tsukahara M, Kurosawa K, Kawame H, Kondoh T, Ohashi H, Tsukino R, Kondoh Y, Shimokawa O, Ida T, Nagai T, Fukushima Y, Yoshiura K, Niikawa N, Matsumoto N. Harada N, et al. Among authors: tsukino r. J Med Genet. 2004 Feb;41(2):130-6. doi: 10.1136/jmg.2003.014639. J Med Genet. 2004. PMID: 14757861 Free PMC article. No abstract available.
Mild form of beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross-reactive material in EB-transformed lymphocytes.
Fukao T, Kodama A, Aoyanagi N, Tsukino R, Uemura S, Song XQ, Watanebe H, Kuhara T, Matsumoto I, Orii T, Kondo N. Fukao T, et al. Among authors: tsukino r. Clin Genet. 1996 Oct;50(4):263-6. doi: 10.1111/j.1399-0004.1996.tb02641.x. Clin Genet. 1996. PMID: 9001814
13 results