P-37 Isochromosome Xq in a Female Infant with Brachmann-de-Lange Phenotype.

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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
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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,
A male with multiple anomalies showing deletion of the D15S986 region derived from his mother(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
An infant of macrocephaly-cutis marmorata telangiectatica congenita with lymphangiectasia
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.
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
Efficacy and Safety of Leukocytapheresis Therapy with Leukocyte Removal Filter for Patients with Primary Biliary Cirrhosis : Liver Disease
The Effect of Different Membrane Materials on Patients with Primary Biliary Cirrhosis Who Have Been Treating by Double Filtration Plasmapheresis(Hepatic Disease,General Presentation,Proceedings of the Thirteenth Annual Meeting of Japanese Society for Aphe
IS-25 Improvement of HPV detectable rate on cytological smears by PCR in situ hybridization
Nuclear and Electronic Sputtering Induced by High Energy Heavy Ions
SI-1 Medical Care in Congenital Malformation Syndromes.(I.PROGRESS AND PROBLEMS IN POSTNATAL TREATMENT OF CONGENITAL ANOMALIES)

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