نتایج جستجو برای: chromosome microdeletions introduction

تعداد نتایج: 492961  

Journal: :Cytogenetic and genome research 2009
A C V Krepischi-Santos D Rajan I K Temple V Shrubb J A Crolla S Huang S Beal P A Otto N P Carter A M Vianna-Morgante C Rosenberg

Chromosome microdeletions or duplications are detected in 10-20% of patients with mental impairment and normal karyotypes. A few cases have been reported of mental impairment with microdeletions comprising tumor suppressor genes. By array-CGH we detected 4 mentally impaired individuals carrying de novo microdeletions sharing an overlapping segment of approximately 180 kb in 17p13.1. This segmen...

Journal: :international journal of reproductive biomedicine 0
majid motovali-bashi zahra rezaei fariba dehghanian halimeh rezaei

background: infertility is a health problem which affects about 10-20% of married couples. male factor infertility is involved approximately 50% of infertile couples. most of male infertility is regarding to deletions in the male-specific region of the y chromosome. objective: in this study, the occurrence of deletions in the azf region and association between infertility and paternal age were ...

Journal: :Annals of the Academy of Medicine, Singapore 2000
E L Yong J Lim Q Wang A Mifsud Y C Ong C K Sim

INTRODUCTION Although infertility affects about 5% of the male population, its cause in most cases is uncertain. Normal spermatogenesis depends on a sequential cascade of genetic events triggered by factors encoded by the sex chromosomes. To determine the contribution of genetic aberrations to male infertility, the X-linked androgen receptor gene and the Y-chromosome were examined for mutations...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2003
S L SãoPedro R Fraietta D Spaine C S Porto M Srougi A P Cedenho M C W Avellar

We determined the prevalence of Y chromosome deletions in a population of 60 Brazilian nonobstructive azoospermic and severely oligozoospermic men. PCR-based screening of microdeletions was performed on lymphocyte DNA for the presence of 14 sequence-tagged sites (STS) located in the azoospermic factor (AZF) on the Yq chromosome. All STS were amplified efficiently in samples from 12 fertile men ...

Journal: :Türk Üroloji Dergisi/Turkish Journal of Urology 2014

2010
Moussa Alkhalaf Kamal Al-Shoumer

Approximately 15% of couples in the reproductive age group worldwide are affected by infertility, and it is estimated that about 40-50% of infertilities are of male origin. Genetic factor accounts for 10-15% of severe male infertility, including chromosomal aberrations and single gene mutations (Ferlin et al, 2006). After the Klinfelter syndrome, Y chromosomal microdeletions are the most freque...

2013
Mohammad Hasan Sheikhha Mohammad Ali Zaimy Saeede Soleimanian Seyed Mehdi Kalantar Azam Rasti Maryam Golzade Hamid Hoseini Fahraji

BACKGROUND It has been hypothesized that Y-q microdeletion can account for significant proportion of infertility in men. There are three nonoverlapping regions referred to as the "azoozpermia factors" AZFa, AZFb, and AZFc from proximal to distal part of Y-q. These have been defined as spermatogenesis loci, this region deletions have been shown to be involved in male azoospermic or severe oligoo...

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