نتایج جستجو برای: microdeletion

تعداد نتایج: 1516  

Journal: :The American Journal of Human Genetics 2019

Journal: :Journal of Medical Case Reports 2018

Journal: :The American journal of psychiatry 1999
C H Chen Y R Lee M Y Chung F C Wei F J Koong C K Shaw J I Yeh K J Hsiao

OBJECTIVE Catechol O-methyltransferase (COMT) is involved in the degradation of catecholamine neurotransmitters. Recent linkage studies of schizophrenia and molecular studies of velocardiofacial syndrome suggest that the COMT gene might be a candidate gene for schizophrenia. METHOD The authors systematically searched for mutations and microdeletion of the COMT gene in 177 Chinese schizophreni...

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...

Journal: :Journal of medical genetics 2010
Lisenka E L M Vissers Bert B A de Vries Joris A Veltman

Structural chromosomal rearrangements can lead to a wide variety of serious clinical manifestations, including mental retardation (MR) and congenital malformations. Over the last few years, rearrangements below the detection level of conventional karyotyping have been proved to contribute significantly to the cause of MR. These so-called copy number variations are now routinely being detected u...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Dirk Prawitt Thorsten Enklaar Barbara Gärtner-Rupprecht Christian Spangenberg Monika Oswald Ekkehart Lausch Peter Schmidtke Dirk Reutzel Stephan Fees Rob Lucito Maria Korzon Izabela Brozek Janusz Limon David E Housman Jerry Pelletier Bernhard Zabel

We have analyzed several cases of Beckwith-Wiedemann syndrome (BWS) with Wilms' tumor in a familial setting, which give insight into the complex controls of imprinting and gene expression in the chromosome 11p15 region. We describe a 2.2-kbp microdeletion in the H19/insulin-like growth factor 2 (IGF2)-imprinting center eliminating three target sites of the chromatin insulator protein CTCF that ...

2015
Akemi J. Tanaka Renkui Bai Megan T. Cho Kwame Anyane-Yeboa Priyanka Ahimaz Ashley L. Wilson Fran Kendall Beverly Hay Timothy Moss Monica Nardini Mislen Bauer Kyle Retterer Jane Juusola Wendy K. Chung

PURA is the leading candidate gene responsible for the developmental phenotype in the 5q31.3 microdeletion syndrome. De novo mutations in PURA were recently reported in 15 individuals with developmental features similar to the 5q31.3 microdeletion syndrome. Here we describe six unrelated children who were identified by clinical whole-exome sequencing (WES) to have novel de novo variants in PURA...

Journal: :Bosnian journal of basic medical sciences 2016
Amina Kurtovic-Kozaric Lejla Mehinovic Meliha Stomornjak-Vukadin Ilvana Kurtovic-Basic Feriha Catibusic Mirza Kozaric Senka Mesihovic-Dinarevic Mensuda Hasanhodzic Darinka Glamuzina

Microdeletion syndromes are caused by chromosomal deletions of less than 5 megabases which can be detected by fluorescence in situ hybridization (FISH). We evaluated the most commonly detected microdeletions for the period from June 01, 2008 to June 01, 2015 in the Federation of Bosnia and Herzegovina, including DiGeorge, Prader-Willi/Angelman, Wolf-Hirschhorn, and Williams syndromes. We report...

2018
Ioulia Gourari Romaine Schubert Aparna Prasad

Copy number variants (CNVs) of 1q21.1 are increasingly being recognized due to the widespread use of genetic screening tests for the investigation of developmental disorders and epilepsy. These include microdeletion and microduplication syndromes, associated with a wide variety of pathology including autism spectrum disorders, attention-deficit disorder, learning disabilities, hypotonia, facial...

2015
Maryam Sedghi Hossein Abdali Mehrdad Memarzadeh Mansoor Salehi Narges Nouri Majid Hosseinzadeh Nayereh Nouri

Misalignments of low-copy repeats (LCRs) located in chromosome 22, particularly band 22q11.2, predispose to rearrangements. A variety of phenotypic features are associated with 22q11.2 microduplication syndrome which makes it challenging for the genetic counselors to recommend appropriate genetic assessment and counseling for the patients. In this study, multiplex ligation probe dependent ampli...

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