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Inverted insertion of chromosome 7q and ectrodactyly.
Naritomi K, Izumikawa Y, Tohma T, Hirayama K. Naritomi K, et al. Among authors: izumikawa y. Am J Med Genet. 1993 Jun 15;46(5):492-3. doi: 10.1002/ajmg.1320460505. Am J Med Genet. 1993. PMID: 8322806
Sanfilippo type B syndrome: five patients with an R565P homozygous mutation in the alpha-N-acetylglucosaminidase gene from the Okinawa islands in Japan.
Chinen Y, Tohma T, Izumikawa Y, Uehara H, Ohta T. Chinen Y, et al. Among authors: izumikawa y. J Hum Genet. 2005;50(7):357-359. doi: 10.1007/s10038-005-0258-4. Epub 2005 Jun 3. J Hum Genet. 2005. PMID: 15933803
Assignment of the human PAX4 gene to chromosome band 7q32 by fluorescence in situ hybridization.
Tamura T, Izumikawa Y, Kishino T, Soejima H, Jinno Y, Niikawa N. Tamura T, et al. Among authors: izumikawa y. Cytogenet Cell Genet. 1994;66(2):132-4. doi: 10.1159/000133684. Cytogenet Cell Genet. 1994. PMID: 8287686
Small interstitial deletion of the long arm of chromosome 2 (2q24.3): further delineation of 2q medial monosomy syndrome.
Chinen Y, Tohma T, Izumikawa Y, Iha T, Goya Y, Naritomi K. Chinen Y, et al. Among authors: izumikawa y. Jpn J Hum Genet. 1996 Sep;41(3):323-8. doi: 10.1007/BF01913175. Jpn J Hum Genet. 1996. PMID: 8996968
Two sisters with Toriello-Carey syndrome.
Chinen Y, Tohma T, Izumikawa Y, Taketomi H, Iha T, Ohta T, Naritomi K. Chinen Y, et al. Among authors: izumikawa y. Am J Med Genet. 1999 Nov 26;87(3):262-4. doi: 10.1002/(sici)1096-8628(19991126)87:3<262::aid-ajmg13>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10564882
Characterization of marker chromosomes by fish using microdissected probes from old Carnoy-fixed cells: report of two cases.
Chinen Y, Tohma T, Izumikawa Y, Naritomi K, Hirayama K. Chinen Y, et al. Among authors: izumikawa y. Jpn J Hum Genet. 1997 Dec;42(4):543-9. doi: 10.1007/BF02767032. Jpn J Hum Genet. 1997. PMID: 9560955
The Costello syndrome: a boy with thick mitral valves and arrhythmias.
Izumikawa Y, Naritomi K, Tohma T, Shiroma N, Hirayama K. Izumikawa Y, et al. Jpn J Hum Genet. 1993 Sep;38(3):329-34. doi: 10.1007/BF01874143. Jpn J Hum Genet. 1993. PMID: 7505126 Review.
16q21 is critical for 16q deletion syndrome.
Naritomi K, Shiroma N, Izumikawa Y, Sameshima K, Ohdo S, Hirayama K. Naritomi K, et al. Among authors: izumikawa y. Clin Genet. 1988 May;33(5):372-5. doi: 10.1111/j.1399-0004.1988.tb03464.x. Clin Genet. 1988. PMID: 3378367
Trisomy 9q3 syndrome: a case report and review of the literature.
Naritomi K, Izumikawa Y, Goya Y, Gushiken M, Shiroma N, Hirayama K. Naritomi K, et al. Among authors: izumikawa y. Clin Genet. 1989 Apr;35(4):293-8. doi: 10.1111/j.1399-0004.1989.tb02947.x. Clin Genet. 1989. PMID: 2653675 Review.
Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7.
Naritomi K, Izumikawa Y, Ohshiro S, Yoshida K, Shimozawa N, Suzuki Y, Orii T, Hirayama K. Naritomi K, et al. Among authors: izumikawa y. Hum Genet. 1989 Dec;84(1):79-80. doi: 10.1007/BF00210677. Hum Genet. 1989. PMID: 2606480
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