Array Comparative Genomic Hybridization (acgh) - Genetic Mutations

Relevant Publications

Papillary renal neoplasm with reverse polarity has low frequency of alterations in chromosomes 7, 17, and Y.

Issue Release: 2024

Cancer Sample Analysis Utilizing Single-Nucleotide Polymorphism Array and Array Comparative Genomic Hybridization.

Issue Release: 2024

Copy number variations in autistic children.

Issue Release: 2024

Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study.

Issue Release: 2024

Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome.

Issue Release: 2024

Low-level mosaic trisomy 21 at amniocentesis and cordocentesis in the second trimester in a pregnancy associated with positive non-invasive prenatal testing for trisomy 21, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome.

Issue Release: 2024

Evaluation of Nanopore Sequencing on Polar Bodies for Routine Pre-Implantation Genetic Testing for Aneuploidy.

Issue Release: 2024

Genomic insights into familial adenomatous polyposis: unraveling a rare case with whole APC gene deletion and intellectual disability.

Issue Release: 2024

Mosaic distal 9p deletion or 46,XY,del(9)(p23)/46,XY at amniocentesis in a pregnancy associated with perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome.

Issue Release: 2024

Subungual melanoma: molecular analysis of 31 cases from early stage to invasive melanoma.

Issue Release: 2024

Added value of whole-exome and RNA sequencing in advanced and refractory cancer patients with no molecular-based treatment recommendation based on a 90-gene panel.

Issue Release: 2024

The Use of CGH Arrays for Identifying Copy Number Variations in Children with Autism Spectrum Disorder.

Issue Release: 2024

Impact of copy number variants in epilepsy plus neurodevelopment disorders.

Issue Release: 2024

Incidental detection of familial 8p23.2 microduplication encompassing CSMD1 associated with mosaic 46,XY,t(7;8)(q31.2;p23.1)/46,XY at amniocentesis in a pregnancy with no apparent phenotypic abnormality and a favorable outcome.

Issue Release: 2024

Current Diagnostic Approaches in the Genetic Diagnosis of Disorders of Sex Development.

Issue Release: 2024

Low-level mosaic trisomy 7 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 7 cell line and a favorable fetal outcome.

Issue Release: 2024

Prenatal diagnosis of a de novo 10p12.1p11.23 microdeletion encompassing the WAC gene in a fetus associated with bilateral hydronephrosis and right clubfoot on prenatal ultrasound.

Issue Release: 2024

Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder loci.

Issue Release: 2024

Low-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, positive non-invasive prenatal testing for trisomy 14, perinatal progressive decrease of the trisomy 14 cell line and a favorable fetal outcome.

Issue Release: 2024

Conventional Cytogenetic Analysis and Array CGH + SNP Identify Essential Thrombocythemia and Prefibrotic Primary Myelofibrosis Patients Who Are at Risk for Disease Progression.

Issue Release: 2024

How Does CRISPR-Cas9 Work?

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What are Common Genetic Factors Involved?

Can Mutations in Non-Coding Regions Cause Diseases?

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How Do Genetic Mutations Affect Immunotherapy?

How Do Deletion Mutations Occur?

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Array Comparative Genomic Hybridization (acgh) - Genetic Mutations

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