Literature DB >> 6609671

Ring-14 and trisomy 14q in the same child.

C Pangalos, V Velissariou, M Ghica, D Liacacos.   

Abstract

The case of a male child with three cell lines is described: one cell line with ring chromosome 14, another trisomic for 14q, due to a derived metacentric 14q;14q, and a third one with a normal male karyotype. The clinical findings are compatible with those of the r(14) syndrome.

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Mesh:

Year:  1984        PMID: 6609671

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  3 in total

Review 1.  Delineation of 14q32.3 deletion syndrome.

Authors:  A P Ortigas; C K Stein; L L Thomson; J J Hoo
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

2.  A somatic origin of homologous Robertsonian translocations and isochromosomes.

Authors:  W P Robinson; F Bernasconi; S Basaran; M Yüksel-Apak; G Neri; F Serville; P Balicek; R Haluza; L M Farah; G Lüleci
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

3.  Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical region.

Authors:  A J Mears; H el-Shanti; J C Murray; H E McDermid; S R Patil
Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025

  3 in total

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