[HTML][HTML] Defining laboratory reference values and decision limits: populations, intervals, and interpretations
JC Boyd - Asian journal of andrology, 2010 - ncbi.nlm.nih.gov
This article provides a brief overview of various approaches that may be utilized for the
analysis of human semen test results. Reference intervals are the most widely used tool for …
analysis of human semen test results. Reference intervals are the most widely used tool for …
[HTML][HTML] Chromosomal and molecular abnormalities in a group of Brazilian infertile men with severe oligozoospermia or non-obstructive azoospermia attending an …
PURPOSE: To determine the frequency of genetic alterations in a population of Brazilian
infertile men with severe oligozoospermia or non-obstructive azoospermia. MATERIALS …
infertile men with severe oligozoospermia or non-obstructive azoospermia. MATERIALS …
Clinical diagnostic Next-Generation sequencing: The case of CFTR carrier screening
YL Loukas, G Thodi, E Molou, V Georgiou… - … journal of clinical and …, 2015 - Taylor & Francis
A 23-mutation panel for CFTR carrier screening is recommended to women of reproductive
age by the American College of Obstetricians and Gynecologists. In the present study the …
age by the American College of Obstetricians and Gynecologists. In the present study the …
Screening of ΔF508 mutation and IVS8‐poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD
M Ghorbel, S Baklouti‐Gargouri, R Keskes… - Andrologia, 2012 - Wiley Online Library
It is well established that cystic fibrosis transmembrane conductance regulator gene (CFTR)
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
mutations are involved in congenital bilateral absence of the vas deferens (CBAVD) …
The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in …
L Jafari, K Safinejad, M Nasiri, M Heidari… - Genes & Genomics, 2023 - Springer
Background Male infertility due to very severe oligozoospermia has been associated with
some genetic risk factors. Objective To investigate the distribution of the mutations in the …
some genetic risk factors. Objective To investigate the distribution of the mutations in the …
精子线粒体DNA 损伤与男性不育
李刚琴， 何映 - 中国优生与遗传杂志, 2010 - cqvip.com
精子线粒体DNA损伤与男性不育-[维普官方网站]-www.cqvip.com-维普网 我的维普 购物车 充值
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High frequency of sex chromosomal disomy in spermatozoa of Lebanese infertile men
BG Younes, KM Hazzouri, MJ Chaaban… - Journal of …, 2011 - Wiley Online Library
In Lebanon, assisted reproductive techniques (ART) are widely used to overcome infertility,
but the genetic risk associated with these techniques is still ignored. In this study, in order to …
but the genetic risk associated with these techniques is still ignored. In this study, in order to …
染色体核型异常男性不育患者Y 染色体微缺失分析
单桂芬， 苏学今， 郑贤红， 常燕， 云馨， 刘睿智 - 中国优生与遗传杂志, 2009 - cqvip.com
目的探讨染色体核型异常与Y 染色体微缺失之间的关系. 方法578 例男性不育患者均来自2007
年6 月至2008 年5 月吉林省生殖医学研究所临床门诊. 所有患者临床表现均为无精子症或严重 …
年6 月至2008 年5 月吉林省生殖医学研究所临床门诊. 所有患者临床表现均为无精子症或严重 …
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 …
Azoospermia Factor (AZF) microdeletions among patients with non-obstructive azoospermia …
Association between MTHFR A1298C polymorphism and male infertility: A meta-analysis
There have been several epidemiological studies evaluating the potential association
between the methylenetetrahydrofolate reductase (MTHFR) A1298C polymorphism and the …
between the methylenetetrahydrofolate reductase (MTHFR) A1298C polymorphism and the …