Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility

Author:

Bahrami Zadegan S.12,Dabbagh Bagheri S.2,Joudaki A.2,Samiee Aref M. H.12,Saeidian A. H.3,Abiri M.24,Zeinali S.25ORCID

Affiliation:

1. Department of Biotechnology; College of Science; University of Tehran; Tehran Iran

2. Dr. Zeinali's Medical Genetics Laboratory; Kawsar Human Genetics Research Center; Tehran Iran

3. Department of Dermatology and Cutaneous Biology; Sidney Kimmel Medical College; Thomas Jefferson University; Philadelphia PA USA

4. Department of Medical Genetics and Molecular Biology; School of Medicine; Iran University of Medical Sciences; Tehran Iran

5. Department of Molecular Medicine; Pasteur Institute of Iran; Biotechnology Research Center; Tehran Iran

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Reference36 articles.

1. 47, XXY (Klinefelter syndrome) and 47, XYY: Estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling;Abramsky;Prenatal Diagnosis,1997

2. Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males;Al-Achkar;Biomedical reports,2013

3. Prevalence of Y chromosome microdeletions in idiopathic azoospermia cases in Central Indian Men;Ambulkar;Journal of Clinical and Diagnostic Research (JCDR),2015

4. Genetic risk of Azoospermia Factor (AZF) microdeletions in idiopathic cases of azoospermia and oligozoospermia in Central Indian population;Ambulkar;Journal of Clinical and Diagnostic Research (JCDR),2014

5. Prenatal and postnatal prevalence of Klinefelter syndrome: A national registry study;Bojesen;The Journal of Clinical Endocrinology & Metabolism,2003

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