Two 48,XXYY patients: clinical, cytogenetic and molecular aspects-Reference-Cited by-同舟云学术

Two 48,XXYY patients: clinical, cytogenetic and molecular aspects

Published:2003-10 Issue:4 Volume:46 Page:479-481
ISSN:0003-3995
Container-title:Annales de Génétique
language:en
Short-container-title:Annales de Génétique

Author:

Zelante L,Piemontese M.R,Francioli G,Calvano S

Publisher

Elsevier BV

Subject

Genetics

Reference16 articles.

1. Metylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human-androgen receptor gene correlates with X-chromosome inactivation;Allen;Am. J. Hum. Genet.,1992

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

3. The 48,XXYY syndrome. Follow-up data on clinical characteristics and pathological findings in 5 patients;Borghraef;Genet. Couns.,1991

4. Venous thromboembolic disease in Klinefelter’s syndrome;Campbell;Curr. Genet.,1981

5. Hypostatic ulceration in Klinefelter’s syndrome;Howell;Br. Med. J.,1978

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