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dc.contributor.authorKOPPERS, B
dc.contributor.authorTERCANLI, S
dc.contributor.authorHOLZGREVE, W
dc.contributor.authorMINY, P
dc.contributor.authorBOGDANOVA, N
dc.contributor.authorREHDER, H
dc.contributor.authorEXELER, R
dc.contributor.authorHORST, J
dc.contributor.authorBASARAN, Seher
dc.contributor.authorDWORNICZAK, B
dc.date.accessioned2021-03-04T11:20:46Z
dc.date.available2021-03-04T11:20:46Z
dc.date.issued1995
dc.identifier.citationMINY P., KOPPERS B., DWORNICZAK B., BOGDANOVA N., HOLZGREVE W., TERCANLI S., BASARAN S., REHDER H., EXELER R., HORST J., "Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally.", American journal of medical genetics, cilt.57, sa.1, ss.102-6, 1995
dc.identifier.issn0148-7299
dc.identifier.othervv_1032021
dc.identifier.otherav_71dc4a09-06dc-4322-ab2c-9a38a8ce7aba
dc.identifier.urihttp://hdl.handle.net/20.500.12627/78377
dc.identifier.urihttps://doi.org/10.1002/ajmg.1320570121
dc.description.abstractThe parental origin of the additional chromosome complement in a total of 17 cases of triploidy was determined mainly using highly polymorphic microsatellites. Maternal origin of the triploidy was demonstrated in most cases. To the best of our knowledge, this is the first systematic evaluation of the parental origin of chromosome sets in fetuses who survived until a cytogenetic diagnosis was established. In contrast to previous investigations this study documented a predominance of maternal origin of the extra haploid set mainly due to longer survival time for digynic triploidies. The concept of 2 distinct fetal phenotypes in triploidy is clearly supported by this study. (C) 1995 Wiley-Liss, Inc.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleParental origin of the extra haploid chromosome set in triploidies diagnosed prenatally.
dc.typeMakale
dc.relation.journalAmerican journal of medical genetics
dc.contributor.department, ,
dc.identifier.volume57
dc.identifier.issue1
dc.identifier.startpage102
dc.identifier.endpage6
dc.contributor.firstauthorID116169


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