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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2013-06-28</publicationDate>
    
        <volume>10</volume>
        <issue>1</issue>

 
    <startPage></startPage>
    <endPage></endPage>

	 
      <doi>10.13005/bbra/1113</doi>
        <publisherRecordId>10312</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Cytogenetic and Y-chromosome Micro-deletions Analysis of Infertile Indian Males with non-obstructive Azoospermia and Severe Oligozoospermia</title>

    <authors>
	 


      <author>
       <name>Mohammad Shahid</name>

 
		
	<affiliationId>1,2</affiliationId>
      </author>
    

	

	

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Biochemistry and Molecular Biology, College of Medicine, Salman bin Abdulaziz University, Alkharj, KSA</affiliationName>
    

		
		<affiliationName affiliationId="2">Human Genetics Laboratory, Department of Biosciences, Jamia Millia Islamia (A Central University), New Delhi, India.</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">This study aimed to determine the frequency and type of chromosome anomalies and Y-chromosome microdeletions in Indian infertile males by using non-obstructive azoospermia and severe oligozoospermia. The study included 168 Indian infertile males. G-banding cytogenetic analysis was performed on the peripheral blood lymphocytes of 91 men with non-obstructive azoospermia and 77 men with oligozoospermia. A molecular genetic analysis of Y-chromosome was also performed with multiplex polymerase chain reaction (M-PCR) amplification by using15 Y-specific sequence-tagged sites (STSs) of azoospermia factor (AZF) region to screen the microdeletions in AZFs region of Y-chromosome. Out of 168 cases, 152 had normal karyotype 46,XY chromosomal constitution. Cytogenetic abnormalities were found in 13 (7.74%) infertile patients. The frequency of chromosomal anomalies for non-obstructive azoospermia 7 (4.16%) was slightly higher than severe oligozoospermia 6 (3.57%). Chromosomal variants werefound in 2.38% patients. The microdeletions of Y-chromosome were observed in 1.19% and 0.59% patients with non-obstructive azoospermia and severe oligozoospermia, respectively. Microdeletions of both AZFa and AZFc genes identified with normal karyotype. This study has provided information that genetic anomalies act as a risk factor for infertility. It is therefore suggested that genetic techniques should be used for diagnosis purpose to obtain the genetic data for possible genetic counseling/cure to minimize the risk of transmitted genetic anomalies.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol10no1/cytogenetic-and-y-chromosome-micro-deletions-analysis-of-infertile-indian-males-with-non-obstructive-azoospermia-and-severe-oligozoospermia/</fullTextUrl>



      <keywords language="eng">
        <keyword>Male infertility; Chromosomal anomalies; Y-chromosome micro-deletion; Azoospermia</keyword>
      </keywords>

  </record>
</records>