Ninomiya S. | Department Of Pediatrics Okayama University Graduate School Of Medicine And Dentistry

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概要

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著作論文

E-3 Molecular studies on parental origin in two patients with de novo trisomy 9_q.
P-37 Isochromosome Xq in a Female Infant with Brachmann-de-Lange Phenotype.
B-03 An Infant with Mixed Gonadal Dysgenesis and Mos 45, X/46, X, idic(Yp)Karyotype Studied for Extent of Mosaicism in the Gonads.
Three cases of unbalanced X/aut translocations : Clinical analysis and inactivation pattern study : The 35th Annual Meeting of the Japanese Teratology Society
SRY gene in two cases with 45,X/46,X, dic(Yq) mosaicism : Abstracts of Papers Presented at the Thirty-Fourth Annual Meeting of the Japanese Teratology Society Kochi, Japan July14-16, 1994
Application of two color fluorescence in situ hybridization (FISH) to prenatal diagnosis of chromosome abnormalities : Abstracts of Papers Presented at the Thirty-Fourth Annual Meeting of the Japanese Teratology Society Kochi, Japan July14-16, 1994
Low percentage mosaicism for trisomy 21 in amniotic fluid cell culture : Application of fluorescence in situ hybridization (FISH) to prenatal diagnosis : Abstracts of Papers Presented at the Thirty-Third Annual Meeting of the Japanese Teratology Society N
Interchange trisomy 9 due to maternal t(6;9) translocation : Abstracts of Papers Presented at the Thirty-Third Annual Meeting of the Japanese Teratology Society Nagoya, Japan, July 21-23, 1993
Chromosome change in r(22) during long-term cell culture : Abstracts of Papers Presented at the Thirty-Third Annual Meeting of the Japanese Teratology Society Nagoya, Japan, July 21-23, 1993
Chromosome mosaicism in amniotic fluid cell culture : Abstracts of Papers Presented at the Thirty-Second Annual Meeting of the Japanese Teratology Society Tokyo, Japan, July 8-10, 1992
Atopic dermatitis in two cases with ring chromosome 18 : Abstracts of Papers Presented at the Thirty-Second Annual Meeting of the Japanese Teratology Society Tokyo, Japan, July 8-10, 1992
A male with multiple anomalies showing deletion of the D15S986 region derived from his mother(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
Case of 46,XY,t(7;11) with bilateral sensorineural deafness, cleft lip and palate, and characteristic face
E-2 Identification of supernumerary r(1) mosaicism using spectral karyotyping (SKY) analysis.
P-38 A de novo17p Trisomy with Anal Atresia Diagnosed by Fluorescent in situ Hybridization.
Nuclear and Electronic Sputtering Induced by High Energy Heavy Ions

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