[HTML][HTML] Y choromosomal microdeletion screening in the workup of male infertility and its current status in India

R Suganthi, VV Vijesh, N Vandana… - International journal of …, 2014 - ncbi.nlm.nih.gov
Spermatogenesis is an essential stage in human male gamete development, which is
regulated by many Y chromosome specific genes. Most of these genes are centred in a …

[HTML][HTML] Basic and clinical genetic studies on male infertility in Iran during 2000-2016: A review

S Moghbelinejad, H Mozdarani… - International Journal …, 2018 - ncbi.nlm.nih.gov
The male factor contributes to 50% of infertility. The cause of male infertility is idiopathic and
could be congenital or acquired. Among different factors which are involved in idiopathic …

[PDF][PDF] Original Research cytogenetic analysis in infertile males with sperm anomalies

EÖ Etem, H Yüce, D Erol, ŞD Deveci… - Marmara …, 2009 - researchgate.net
Objective: In a half of all childless partnerships the infertility is caused by the male.
Chromosomal abnormalities are more prevalent in infertile men compared to fertile men …

Cytogenetic studies among Iranian infertile men: The first 20-year long-term report

C Azimi, M Khaleghian, F Farzanfar - African Journal of Biotechnology, 2012 - ajol.info
Chromosomal aberrations have been postulated to be one of the principal genetic factors in
male infertility and occur in about 2 to 3% of unselected patients with proven sub-fertility …

The genetic causes of male infertility in Iranian population; a systematic review

F Azizi, MD Omrani, MAS Gilani… - Men's Health Journal, 2018 - journals.sbmu.ac.ir
Introduction: Infertility affects an estimated 15% of couples globally and in Iran, a quarter of
couples experiences primary infertility. Males are found to be individually responsible for 20 …

[HTML][HTML] A rare de novo complex chromosomal rearrangement (CCR) involving four chromosomes in an oligo-asthenosperm infertile man

S Asia, HV Nasab, M Sabbaghian, H Kalantari… - Cell Journal …, 2014 - ncbi.nlm.nih.gov
Complex chromosomal rearrangements (CCRs) are rare events involving more than two
chromosomes and over two breakpoints. They are usually associated with infertility or sub …

Homologous Robertsonian translocations: spectrum, sex ratios, and reproductive risks

NV Kovaleva - Russian Journal of Genetics, 2019 - Springer
Robertsonian translocations/isochromosomes formed by homologous acrocentric
chromosomes are rare, and consequently their epidemiology has not been well …

[HTML][HTML] Sex chromosome aneuploidy in cytogenetic findings of referral patients from south of Iran

N Jouyan, ED Dehaghani, S Senemar… - Iranian Journal of …, 2012 - ncbi.nlm.nih.gov
Background: Chromosome abnormality (CA) including Sex chromosomes abnormality
(SCAs) is one of the most important causes of disordered sexual development and infertility …

[PDF][PDF] Frequency of Chromosomal Abnormalities in Subpopulations of Infertile Males among Chinese Hakka Population

P Zhao, X Gu, H Wang, M Yang - Journal of Molecular and …, 2018 - scholar.archive.org
The frequency of chromosomal abnormalities is supposed to be elevated in infertile males
as well as shown negative correlation of sperm concentration. Cytogenetic analysis …

The Frequency of Chromosomal Abnormalities and Y Chromosome Microdeletions in Infertile Non-Obstructive Azoospermic and Severe Oligozoospermic Males

MM Abdel-Razek, ES Elsobky, YM Moustafa… - Human …, 2017 - journals.ekb.eg
Purpose: To estimate the frequency and types of both chromosomal abnormalities and
Azoospermia Factor (AZF) microdeletions among patients with non-obstructive azoospermia …