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   <subfield code="a">10.1007/s10815-011-9542-8</subfield>
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   <subfield code="a">Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Haluk Akin, Huseyin Onay, Emre Turker, Ferda Ozkinay]</subfield>
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   <subfield code="a">Purpose: To detect somatic cytogenetic abnormalities and AZF microdeletions in a sample of 187 Turkish infertile men to determine the frequencies and the characteristics of our primary male infertility data in order to perform appropriate genetic counseling. Methods: This study included 187 infertile men. Chromosomal studies and screening of AZF deletions was performed by multiplex polymerase chain reaction (PCR) analysis using the Y Chromosome Deletion Detection System. Results: Cytogenetic study revealed chromosomal abnormality in 9 subjects (4.8%). In remaining 178 subjects, 7 subjects (3.93%) were detected to have Y chromosome microdeletions. The AZFc region was the most frequently involved region in microdeletion process in affected subjects. All subjects having microdeletion were azoospermic Conclusions: Cytogenetic and molecular study should be performed to obtain reliable genetic information for the genetic counseling of primary infertile man. Y chromosome microdeletion diagnosis is useful in decision making for assisted reproductive technics.</subfield>
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   <subfield code="a">Primary male infertiliy</subfield>
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   <subfield code="t">Journal of Assisted Reproduction and Genetics</subfield>
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