Literature DB >> 5567399

Radioulnar synostosis. A common occurrence in sex chromosomal abnormalities.

J Jancu.   

Abstract

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Year:  1971        PMID： 5567399

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  2 in total

1.  Familial radioulnar synostosis.

Authors:  R A Spritz
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

2.  A rare 47 XXY/46 XX mosaicism with clinical features of Klinefelter syndrome.

Authors:  Noor Shafina Mohd Nor; Muhammad Yazid Jalaludin
Journal:  Int J Pediatr Endocrinol       Date:  2016-06-02
  2 in total

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