Literature DB >> 7180880

49,XXXXY syndrome.

P D Pallister.   

Abstract

Entities:  

Mesh：

Year:  1982        PMID： 7180880     DOI： 10.1002/ajmg.1320130320

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

1.  First Report of Two Rare Entities in a Family: 49,XXXXY and 45,X.

Authors:  Yavuz Şahin; Aysegül Özcan
Journal:  J Pediatr Genet       Date:  2017-01-18

2.  Congenital knee dislocation in a 49,XXXXY boy.

Authors:  R H Sijmons; A J van Essen; J D Visser; M Iprenburg; G F Nelck; M L Vos-Bender; B de Jong
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

3.  Brief report: a case study of an adolescent male with XXXXY Klinefelter's syndrome.

Authors:  M K Sheridan; S Radlinski
Journal:  J Autism Dev Disord       Date:  1988-09

4.  49,XXXXY: a distinct phenotype. Three new cases and review.

Authors:  J Peet; D D Weaver; G H Vance
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318
  4 in total

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