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

Author:

Butt A M,Mehta D,Goodeve J A,Flinter F A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder;Berberich, M.S.; Carey, J.C.; Lawce, H.J.; Hall, B.D.;Birth Defects,1978

2. Partial trisomy 17q;Fryns, J.P.; Parloir, C.; Van den Berghe, H.;Hum Genet,1979

3. Distal trisomy 17q;Turleau, C.; de Grouchy, J.; Bouveret, J.P.;Clin Genet,1979

4. Brief clinical report: an infant with duplication of 17q21-17qter;Gallien, J.U.; Neu, R.L.; Wynn, R.J.; Steinberg-Warren, N.; Bannermann, R.M.;Am J Med Genet,1981

5. A child with partial trisomy of chromosome 17q and partial monosomy of chromosome 3;Shawe, D.J.; Fear, C.; Appleyard, W.J.;J Med Genet,1983

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1. Clinical and Molecular Cytogenetic Characterization of 2 Sibling Cases with 17q25 Duplication due to Unbalanced Translocation;Molecular Syndromology;2024-05-30

2. Chromosomes and the Skin;Harper's Textbook of Pediatric Dermatology;2011-05-24

3. K;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

4. Opitz “C” trigonocephaly-like syndrome in a patient with terminal deletion of 2p and partial duplication of 17q;American Journal of Medical Genetics Part A;2004-11-11

5. Characterization of a supernumerary marker derived from chromosome 17 by microdissection in an adult with MR/MCA;American Journal of Medical Genetics;1998-04-28

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