Literature DB >> 1161403

Congenital heart disease in 49, XXXXY syndrome.

R B Karsh.   

Abstract

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Year:  1975        PMID： 1161403

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  5 in total

1.  Identification of novel candidate gene loci and increased sex chromosome aneuploidy among infants with conotruncal heart defects.

Authors:  Kazutoyo Osoegawa; David M Iovannisci; Bin Lin; Christina Parodi; Kathleen Schultz; Gary M Shaw; Edward J Lammer
Journal:  Am J Med Genet A       Date:  2013-10-11       Impact factor: 2.802

2.  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

3.  Total anomalous origin of the coronary arteries from the pulmonary artery.

Authors:  S A Heifetz; M Robinowitz; K H Mueller; R Virmani
Journal:  Pediatr Cardiol       Date:  1986       Impact factor: 1.655

4.  Epiphysial dysplasia: a constant finding in the XXXXY syndrome.

Authors:  R Schmidt; M Pajewski; M Rosenblatt
Journal:  J Med Genet       Date:  1978-08       Impact factor: 6.318

5.  An infant with 49XXXXY syndrome: a case report.

Authors:  N P G C R Naotunna; C Liyanage; N Atapattu
Journal:  J Med Case Rep       Date:  2021-12-30
  5 in total

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