Literature DB >> 389192

[Autosomal chromosome aberrations].

A Schinzel.   

Abstract

Mesh：

Year:  1979        PMID： 389192

Source DB:  PubMed          Journal:  Arch Genet (Zur)        ISSN： 0300-984X


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  6 in total

1.  Partial trisomy 13q21toqter de novo due to a recombinant chromosome rec(13)dup q.

Authors:  M Habedank
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

2.  The pathology of trisomy 13 syndrome. A study of 12 cases.

Authors:  P Moerman; J P Fryns; K van der Steen; A Kleczkowska; J Lauweryns
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

3.  Monosomy 18p and pure trisomy 18p in a family with translocation (7;18).

Authors:  M Habedank; G Trost-Brinkhues
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

4.  Duplication of the short arm of chromosome 9. Analysis of five cases.

Authors:  C Cuoco; G Gimelli; F Pasquali; L Poloni; O Zuffardi; P Alicata; G Battaglino; F Bernardi; R Cerone; M Cotellessa; A Ghidoni; S Motta
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

5.  Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Authors:  Ariana Kariminejad; Roxana Kariminejad; Azadeh Moshtagh; Maryam Zanganeh; Mohammad Hassan Kariminejad; Stefan Neuenschwander; Michal Okoniewski; Eva Wey; Albert Schinzel; Alessandra Baumer
Journal:  Eur J Hum Genet       Date:  2011-02-16       Impact factor: 4.246

6.  Uniparental disomy is a chromosomic disorder in the first place.

Authors:  Thomas Liehr
Journal:  Mol Cytogenet       Date:  2022-02-17       Impact factor: 2.009
  6 in total

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