نتایج جستجو برای: chromosome microdeletions introduction

تعداد نتایج: 492961  

Objective Y chromosome deletions (YCDs) in azoospermia factor (AZF) region are associated with abnormal spermatogenesis and may lead to azoospermia or severe oligozoospermia. Assisted reproductive technologies (ART) by intracytoplasmic sperm injection (ICSI) and testicular sperm extraction (TESE) are commonly required for infertility management of patients carrying YCDs. The aim of this study w...

Journal: :Developmental medicine and child neurology 2012
Russell C Dale Padraic Grattan-Smith Michelle Nicholson Greg B Peters

AIM Chromosome microarray (CMA) can determine copy number variants such as microdeletions or microduplications. Microdeletions of movement disorder genes including epsilon-sarcoglycan (SGCE) and thyroid transcription factor-1 (TITF1) have been described in patients with myoclonus dystonia and benign hereditary chorea respectively. We examined whether CMA is a valuable tool in the investigation ...

Journal: :Genetics and molecular research : GMR 2016
X G Liu H Y Hu Y H Guo Y P Sun

Dyszoospermia due to genetic factors is the leading cause of male infertility. To explore the correlation between azoospermia factor (AZF) microdeletion of the Y chromosome and male infertility, we evaluated AZF microdeletion on the long arm of the Y chromosome in 166 infertile males and 50 fertile males using multiplex polymerase chain reactions amplification and gel electrophoresis. The resul...

2014
Dana Mierla Dumitru Jardan Veronica Stoian

BACKGROUND Chromosomal abnormalities and Y chromosome microdeletions are regarded as two most frequent genetic causes associated with failure of spermatogenesis in the Caucasian population. MATERIALS AND METHODS To investigate the distribution of genetic defects in the Romanian population with azoospermia or severe oligozoospermia, karyotype analysis by G-banding was carried out in 850 idiopa...

Journal: :American journal of medical genetics. Part C, Seminars in medical genetics 2010
Karin Buiting

Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are two distinct neurogenetic disorders in which imprinted genes on the proximal long arm of chromosome 15 are affected. Although the SNORD116 gene cluster has become a prime candidate for PWS, it cannot be excluded that other paternally expressed genes in the chromosomal region 15q11q13 contribute to the full phenotype. AS is caused by a d...

2014
Adrian Mc Cormack Juliet Taylor Leah Te Weehi Donald R Love Alice M George

Concurrent cryptic microdeletion and microduplication syndromes have recently started to reveal themselves with the advent of microarray technology. Analysis has shown that low-copy repeats (LCRs) have allowed chromosome regions throughout the genome to become hotspots for nonallelic homologous recombination to take place. Here, we report a case of a 7.5-year-old girl who manifests microcephaly...

2015
Dennis Lal Ann-Kathrin Ruppert Holger Trucks Herbert Schulz Carolien G. de Kovel Dorothée Kasteleijn-Nolst Trenité Anja C. M. Sonsma Bobby P. Koeleman Dick Lindhout Yvonne G. Weber Holger Lerche Claudia Kapser Christoph J. Schankin Wolfram S. Kunz Rainer Surges Christian E. Elger Verena Gaus Bettina Schmitz Ingo Helbig Hiltrud Muhle Ulrich Stephani Karl M. Klein Felix Rosenow Bernd A. Neubauer Eva M. Reinthaler Fritz Zimprich Martha Feucht Rikke S. Møller Helle Hjalgrim Peter De Jonghe Arvid Suls Wolfgang Lieb Andre Franke Konstantin Strauch Christian Gieger Claudia Schurmann Ulf Schminke Peter Nürnberg Thomas Sander

Genetic generalised epilepsy (GGE) is the most common form of genetic epilepsy, accounting for 20% of all epilepsies. Genomic copy number variations (CNVs) constitute important genetic risk factors of common GGE syndromes. In our present genome-wide burden analysis, large (≥ 400 kb) and rare (< 1%) autosomal microdeletions with high calling confidence (≥ 200 markers) were assessed by the Affyme...

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