Literature DB >> 317780

Two cases of partial trisomy 10q in the same family caused by parental direct insertion [ins. (15;10) (q15;q24q26)].

E Back, J Kosmützky, A Schuwald, H Hameister.   

Abstract

Mesh：

Year:  1979        PMID： 317780

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


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  3 in total

1.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

Review 2.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

3.  Confirmation of a de novo duplication, dup(10)(q24 leads to q26), by GOT1 gene dosage studies.

Authors:  D J Tomkins; B J Gitelman; M H Roberts
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  3 in total

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