Literature DB >> 11043432

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.

J M De Pater1, J P Van Tintelen, R Stigter, H A Brouwers, J M Scheres.   

Abstract

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p: We report on a girl with multiple congenital abnormalities and a prenatally diagnosed 46,XX,14p+ de novo karyotype. Fluorescence in situ hybridization (FISH) demonstrated that the extra material on the short arm of chromosome 14 was not just a polymorphism, but that it originated from chromosome 17. The phenotypic findings of this patient with pure trisomy 17p are compared with those of ten previously published cases.

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Year:  2000        PMID: 11043432

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  2 in total

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Journal:  Hum Genet       Date:  2006-06-22       Impact factor: 4.132

2.  Cystic Dilation of the Aqueductus Sylvii in Case of Trisomy 17p11.2-pter with the Deletion of the Terminal Portion of the Chromosome 6.

Authors:  Emese Horváth; János Sikovanyecz; Attila Pál; László Kaiser; Bálint L Bálint; Póliska Szilárd; Zoltán Kozinszky; János Szabó
Journal:  Case Rep Med       Date:  2011-01-16
  2 in total

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