Literature DB >> 1577463

Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY.

B Van der Auwera1, N Van Roy, A De Paepe, J R Hawkins, I Liebaers, S Castedo, J Dumon, F Speleman.   

Abstract

XX maleness is the most common condition in which testes develop in the absence of a cytogenetically detectable Y chromosome. Using molecular techniques, it is possible to detect Yp sequences in the majority of XX males. In this study, we could detect Y-specific sequences, including the sex-determining region of the Y chromosome (SRY), using fluorescence in situ hybridization. In 5 out of 6 previously unpublished XX males, SRY was translocated onto the terminal part of an X chromosome. This is the first report in which translocation of an SRY-bearing fragment to an X chromosome in XX males could be directly demonstrated.

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Year:  1992        PMID: 1577463     DOI: 10.1007/bf00207036

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  45 in total

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Journal:  Lancet       Date:  1959-04-04       Impact factor: 79.321

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Authors:  M A Ferguson-Smith; A Cooke; N A Affara; E Boyd; J L Tolmie
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

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Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

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Journal:  Lancet       Date:  1966-08-27       Impact factor: 79.321

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Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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Journal:  Hum Genet       Date:  1987-08       Impact factor: 4.132

9.  A deletion map of the human Y chromosome based on DNA hybridization.

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Journal:  Am J Hum Genet       Date:  1986-02       Impact factor: 11.025

10.  A possible common origin of "Y-negative" human XX males and XX true hermaphrodites.

Authors:  N E Abbas; J E Toublanc; C Boucekkine; M Toublanc; N A Affara; J C Job; M Fellous
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

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1.  Sox3 is required for gonadal function, but not sex determination, in males and females.

Authors:  Jeffrey Weiss; Joshua J Meeks; Lisa Hurley; Gerald Raverot; Andrea Frassetto; J Larry Jameson
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

2.  Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

Authors:  E Margarit; A Soler; A Carrió; R Oliva; D Costa; T Vendrell; J Rosell; F Ballesta
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

Review 3.  A multi-faceted approach to understanding male infertility: gene mutations, molecular defects and assisted reproductive techniques (ART).

Authors:  Eisa Tahmasbpour; Dheepa Balasubramanian; Ashok Agarwal
Journal:  J Assist Reprod Genet       Date:  2014-08-13       Impact factor: 3.412

4.  Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

Review 5.  [Genetics of human sex determination and its disturbances].

Authors:  A Braun; U Kuhnle; H Cleve
Journal:  Naturwissenschaften       Date:  1994-07

6.  Genetic characterization of two 46,XX males without gonadal ambiguities.

Authors:  Agata Minor; Fawziah Mohammed; Alla Farouk; Chiho Hatakeyama; Karynn Johnson; Victor Chow; Sai Ma
Journal:  J Assist Reprod Genet       Date:  2008-10-30       Impact factor: 3.412

Review 7.  The epidemiology and etiology of azoospermia.

Authors:  Marcello Cocuzza; Conrado Alvarenga; Rodrigo Pagani
Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365

  7 in total

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