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
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
- 1987-09-30
著者
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Narahara K.
Department Of Pediatrics Okayama Red Cross General Hospital
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NANBA H.
Departments of Pediatrics and Obstetrics, Okayama University Medical School
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KIMOTO H.
Department of Pediatrics, and Department of Urology, Faculty of Medicine, Okayama University
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Hiramoto K.
Asahigawa Jidoin Hospital For Handicapped Children And Department Of Pediatrics Faculty Of Medicine
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Kikkawa K.
Department Of Pediatrics Okayama University Medical School Okayama And Department Of Pediatrics Koch
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Nakahara K.
Asahigawa Jidoin Hosp. Dept. Pediatr. Okayama Univ. And Dept. Radiol. Okayama Red Cross Hosp.
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AKAZAI A.
Department of Pediatrics, Okayama University, School of Medicine
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Akazai A.
Department Of Pediatrics Okayama University School Of Medicine
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Kikkawa K.
Department Of Pediatrics And Department Of Urology Faculty Of Medicine Okayama University
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Nanba H.
Department Of Pediatrics Okayama University Medical School
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Kikkawa K.
Department Of Pediatrics Okayama University Medical School Okayama And Department Of Pediatrics Koch
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Narahara K.
Department Of Pediatrics Okayama University School Of Medicine And Department Of Pediatrics Kochi Prefectural Central Hospital
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NANBA H.
Department of Pediatrics, Okayama University, School of Medicine
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