Abe K - Search Results

1

Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.

Coêlho KE, Egashira M, Kato R, Fujimoto M, Matsumoto N, Rerkamnuaychoke B, Abe K, Harada N, Ohashi H, Fukushima Y, Niikawa N. Coêlho KE, et al. Among authors: abe k. Am J Med Genet. 1996 Jun 14;63(3):468-71. doi: 10.1002/(SICI)1096-8628(19960614)63:3<468::AID-AJMG10>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8737654

2

Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome.

Abe K, Kajii T, Niikawa N. Abe K, et al. Hum Genet. 1989 Jul;82(4):313-6. doi: 10.1007/BF00273988. Hum Genet. 1989. PMID: 2525515

3

Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).

Ishikiriyama S, Tonoki H, Shibuya Y, Chin S, Harada N, Abe K, Niikawa N. Ishikiriyama S, et al. Among authors: abe k. Am J Med Genet. 1989 Aug;33(4):505-7. doi: 10.1002/ajmg.1320330419. Am J Med Genet. 1989. PMID: 2596512

4

Trisomy 13/trisomy 18 mosaicism in an infant.

Abe K, Harada N, Itoh T, Hirakawa O, Niikawa N. Abe K, et al. Clin Genet. 1996 Nov;50(5):300-3. doi: 10.1111/j.1399-0004.1996.tb02378.x. Clin Genet. 1996. PMID: 9007314

5

Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus.

Harada N, Abe K, Nishimura T, Sasaki K, Ishikawa M, Fujimoto M, Matsumoto T, Niikawa N. Harada N, et al. Among authors: abe k. Am J Med Genet. 1998 Feb 3;75(4):432-7. doi: 10.1002/(sici)1096-8628(19980203)75:4<432::aid-ajmg17>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482654

6

Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs.

Deng HX, Abe K, Kondo I, Tsukahara M, Inagaki H, Hamada I, Fukushima Y, Niikawa N. Deng HX, et al. Among authors: abe k. Hum Genet. 1991 Apr;86(6):541-4. doi: 10.1007/BF00201538. Hum Genet. 1991. PMID: 1673956

7

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2.

Niikawa N, Deng HX, Abe K, Harada N, Okada T, Tsuchiya H, Akaboshi I, Matsuda I, Fukushima Y, Kaneko Y, et al. Niikawa N, et al. Among authors: abe k. Hum Genet. 1991 Sep;87(5):561-6. doi: 10.1007/BF00209012. Hum Genet. 1991. PMID: 1680787

8

Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.

Hamabe J, Fukushima Y, Harada N, Abe K, Matsuo N, Nagai T, Yoshioka A, Tonoki H, Tsukino R, Niikawa N. Hamabe J, et al. Among authors: abe k. Am J Med Genet. 1991 Oct 1;41(1):54-63. doi: 10.1002/ajmg.1320410116. Am J Med Genet. 1991. PMID: 1683159

9

Penta X syndrome: a case report with review of the literature.

Kassai R, Hamada I, Furuta H, Cho K, Abe K, Deng HX, Niikawa N. Kassai R, et al. Among authors: abe k. Am J Med Genet. 1991 Jul 1;40(1):51-6. doi: 10.1002/ajmg.1320400110. Am J Med Genet. 1991. PMID: 1887850 Review.

10

De novo interstitial deletion of 1p (pter----p34.1::p32.3----qter).

Yoshino M, Watanabe Y, Harada N, Abe K. Yoshino M, et al. Among authors: abe k. J Med Genet. 1991 Aug;28(8):539-40. doi: 10.1136/jmg.28.8.539. J Med Genet. 1991. PMID: 1920371 Free PMC article.

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