Literature DB >> 26860518

Diagnosis of turner syndrome in two mothers following their daughters' diagnosis.

M Pilar Bahíllo-Curieses1, Sofía Galbis-Soto2, M Concepción Mombiedro-Arizmendi2.   

Abstract

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Year:  2016        PMID： 26860518     DOI： 10.1007/s12020-016-0879-8

Source DB:  PubMed          Journal:  Endocrine        ISSN： 1355-008X            Impact factor:   3.633


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  3 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.  Del (X)(p21.2) in a mother and two daughters with variable ovarian function.

Authors:  A R Zinn; B Ouyang; J L Ross; S Varma; M Bourgeois; V Tonk
Journal:  Clin Genet       Date:  1997-10       Impact factor: 4.438

3.  Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.

Authors:  Marie-France Portnoï; Sandra Chantot-Bastaraud; Sophie Christin-Maitre; Bruno Carbonne; Marie-Paule Beaujard; Boris Keren; Jonathan Lévy; Marc Dommergues; Sylvie Cabrol; Capucine Hyon; Jean-Pierre Siffroi
Journal:  Eur J Med Genet       Date:  2012-07-15       Impact factor: 2.708
  3 in total

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