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A male patient with 48,XXYY syndrome: importance of distinction from Klinefelter's syndrome

  • Published:2008-06-28 Issue:1 Volume:38 Page:74-78
  • ISSN:0009-9163
  • Container-title:Clinical Genetics
  • language:en
  • Short-container-title:

Author:

Grammatico Paola,Bottoni Ugo,Sanctis Stefania,Sulli Nicoletta,Tonanzi Tiziano,Onorio Antonio Carlesimo,Porto Giuseppe

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference16 articles.

1. Ulcères de jambe post-phlébitiques et caryotype XYY: tests de fibrinolyse et fonction androgénique;Bennet;Ann. Dermatol. Venerol.,1987

2. The influence of some drugs on platelet aggregation and adhesion;Bielawiec;Acta. Univ. Carol. MED (Praha),1972

3. Genetic and endocrine findings in a 48,XXYY male;Bloomgarden;JCEM,1980

4. Venous lipodermatosclerosis: treatment by fibrinolytic enhancement and elastic compression;Burnand;Br. Med. J.,1980

5. Venous thromboembolic disease in Klinefelter's syndrome;Campbell;Curr. Genet.,1981

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Leg ulcers associated with Klinefelter's syndrome: a case report and review of the literature;International Wound Journal;2011-08-19

2. Congenital heart disease in the 48,XXYY syndrome;Clinical Genetics;2008-06-28

3. A new look at XXYY syndrome: Medical and psychological features;American Journal of Medical Genetics Part A;2008

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

5. Two 48,XXYY patients: clinical, cytogenetic and molecular aspects;Annales de Génétique;2003-10
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