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Y microdeletion determination for infertile men

The molecular diagnosis of Y-chromosomal microdeletions is a common routine genetic test which is part of the diagnostic workup of azoospermic and severe oligozoospermic men. Microdeletions occur in about one in 4000 men in the general population but its frequency is significantly increased among infertile men (Krausz C, 2014).

Contacts and Location

Contact 1 Linda Piekuse
Contact 2 Linda Gabrusenoka
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Organisational Unit Rīga Stradiņš University
    Scientific Laboratory of Molecular Genetics - Latvia, Rīga

Description

The molecular diagnosis of Y-chromosomal microdeletions is a common routine genetic test which is part of the diagnostic workup of azoospermic and severe oligozoospermic men. Microdeletions occur in about one in 4000 men in the general population but its frequency is significantly increased among infertile men (Krausz C, 2014).

Specification

Sample DNA or material for DNA isolation. For patients DNA sample microdeletions of the regions AZFa (markers sY84, sY86) AZFb (markers sY127, sY134) and AZFc (sY254, sY255) according to EMQN and EAA guidelines (Krausz C, 2014).

Accreditation

EMQN approved EQA sertificate for analysis of Y microdeletions (www.emqn.org).

Delivery time

Negotiable. Depends on many factors: for example, number of samples.

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