Literature DB >> 11746034

Atypical phenotype in a female with a large Xp deletion.

N S Thomas, S M Huson.   

Abstract

Mesh：

Year:  2001        PMID： 11746034

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


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  2 in total

1.  A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions.

Authors:  K L Lachlan; S Youings; T Costa; P A Jacobs; N S Thomas
Journal:  Hum Genet       Date:  2005-11-08       Impact factor: 4.132

2.  Whole Xp Deletion in a Girl with Mental Retardation, Epilepsy, and Biochemical Features of OTC Deficiency.

Authors:  K Joost; P Tammur; R Teek; O Zilina; M Peters; M Kreile; B Lace; R Zordania; I Talvik; K Ounap
Journal:  Mol Syndromol       Date:  2011-09-14
  2 in total

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