SI-1 Medical Care in Congenital Malformation Syndromes.(I.PROGRESS AND PROBLEMS IN POSTNATAL TREATMENT OF CONGENITAL ANOMALIES)
スポンサーリンク
概要
- 論文の詳細を見る
- 日本先天異常学会の論文
- 1999-09-30
著者
-
Narahara K.
Department Of Pediatrics Okayama Red Cross General Hospital
-
NARAHARA K.
Department of Pediatrics, Okayama Red Cross General Hospital
関連論文
- 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.
- B-02 Sexual Ambiguity in a Newborn Boy with a de novo Trisomy 6q.
- Parental Origin of de novo 9p Duplication In Two Cases with Trisomy 9p Syndrome : Paper Presented from Platform
- 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
- Study of the fragile X syndrome in institutionalized retarded males with behavioral disorder : 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
- Peculiar phenotypic abnormalities in a patient with a de novo balanced reciproeal translocation [t(18q;19q)] : Abstracts of Papers Presented at the Thirty-Second Annual Meeting of the Japanese Teratology Society Tokyo, Japan, July 8-10, 1992
- 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
- Chromosome analysis of amniotic fluid cells in fetal anomalies : Abstracts of Papers Presented at the Thirty-First Annual Meeting of the Japanese Teratology Society Izumo, Japan, July 11-12, 1991
- Hypopigmentation of the skin and hair in two cases with distal 2q trisomy : Abstracts of Papers Presented at the Thirty-First Annual Meeting of the Japanese Teratology Society Izumo, Japan, July 11-12, 1991
- Reproductive risk in mating between translocation carriers : Abstracts of Papers Presented at the Thirtieth Annual Meeting of the Japanese Teratology Society Miyazaki, Japan, July 12-13, 1990
- Association of partial agenesis of the corpus callosum with midline lipoma in a case with trisomy 8 mosaicism : Abstracts of Papers Presented at the Thirtieth Annual Meeting of the Japanese Teratology Society Miyazaki, Japan, July 12-13, 1990
- Dicentric Yq chromosome in a male with azoospermia : Abstracts of Papers Presented at the 29th Annual Meeting of the Japanese Teratology Society, Yamagata, Japan July 13 - 14
- Variability in responsiveness of cells to 5'-fluoro-deoxyuridine (FUdr) in fra(X) expression : Abstracts of Papers Presented at the 29th Annual Meeting of the Japanese Teratology Society, Yamagata, Japan July 13 - 14
- Partial deficiency of coagulation factors VII and X in a case with a ring chromosome 13, and the assignment of F7 and F10 to 13q3408→qter : ABSTRACTS OF PAPERS PRESENTED at the TWENTY-SEVENTH ANNUAL MEETING of the JAPANESE TERATOLOGY SOCIETY TOKYO, JAPAN,
- Genetic heterogeneity in spondylocostal dysplasia (SCD): Report of two unrelated cases : ABSTRACTS OF PAPERS PRESENTED at the TWENTY-SEVENTH ANNUAL MEETING of the JAPANESE TERATOLOGY SOCIETY TOKYO, JAPAN, JULY 17-18, 1987
- Regional assignment of the gene locus for craniosynostosis to 7p21.2 : ABSTRACTS OF PAPERS PRESENTED at the TWENTY-SEVENTH ANNUAL MEETING of the JAPANESE TERATOLOGY SOCIETY TOKYO, JAPAN, JULY 17-18, 1987
- SI-1 Medical Care in Congenital Malformation Syndromes.(I.PROGRESS AND PROBLEMS IN POSTNATAL TREATMENT OF CONGENITAL ANOMALIES)