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Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient.
Marquet, Valentine; Bourgeois, Dominique; De Mas, Philippe; Bouneau, Laurence; Vigouroux-Castera, Adeline; Molignier, Romain; Calvas, Patrick.
Afiliación
  • Marquet V; Service de Génétique Médical, Centre Hospitalier Universitaire Purpan Toulouse, France.
  • Bourgeois D; Service de Génétique Médical, Centre Hospitalier Universitaire Purpan Toulouse, France.
  • De Mas P; Laboratoire de Biologie Clinique, Clinique Saint Jean Languedoc Toulouse, France.
  • Bouneau L; Service de Génétique Médical, Centre Hospitalier Universitaire Purpan Toulouse, France.
  • Vigouroux-Castera A; Service de Génétique Médical, Centre Hospitalier Universitaire Purpan Toulouse, France.
  • Molignier R; Laboratoire de Biologie Clinique, Clinique Saint Jean Languedoc Toulouse, France.
  • Calvas P; Service de Génétique Médical, Centre Hospitalier Universitaire Purpan Toulouse, France.
Clin Case Rep ; 3(9): 757-61, 2015 Sep.
Article en En | MEDLINE | ID: mdl-26401282
ABSTRACT
We report on a phenotypically normal 41-year-old azoospermic man with a 45 chromosomes karyotype including one normal chromosome 21, one normal chromosome 22, and a der(22)ins(22;21). Array CGH showed a 1.8 Mb terminal deletion of bands 21pter to 21q21.1 and a 341 kb terminal deletion on band 21q22.3.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2015 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Case Rep Año: 2015 Tipo del documento: Article País de afiliación: Francia
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