Literature DB >> 3874592

De novo distal trisomy 17q.

E Orye, H van Bever.   

Abstract

A boy is described, who shares many of the clinical features found in the few patients with a partial 17q trisomy known at present. Karyotyping revealed a de novo 17q+ chromosome, interpretable as a tandem duplication of the distal long arm region 17q25.

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Mesh:

Year:  1985        PMID: 3874592

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


  5 in total

Review 1.  Sibs lacking characteristic features of duplication of distal 17q.

Authors:  S Ohdo; H Madokoro; T Sonoda; K Ohba
Journal:  J Med Genet       Date:  1989-07       Impact factor: 6.318

2.  Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome.

Authors:  A Serotkin; J Stamberg; L Waber
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

3.  Duplication of distal 17q from a maternal translocation: an additional case with some unique features.

Authors:  A Caine; D M Knapton; R F Mueller; P J Congdon; D Haigh
Journal:  J Med Genet       Date:  1989-09       Impact factor: 6.318

4.  Probable de novo 17q duplication (q11.2-->q21.1): a newly recognised chromosomal syndrome in a child with Klinefelter's syndrome.

Authors:  A M Butt; D Mehta; J A Goodeve; F A Flinter
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

5.  A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literature.

Authors:  Jariya Upadia; Joseph B Philips; Nathaniel H Robin; Edward J Lose; Fady M Mikhail
Journal:  Clin Case Rep       Date:  2018-02-14
  5 in total

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