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Molecular genetics is the study of chromosomes and DNA at the molecular level using DNA technology, whereas cytogenetics is the study of the number and structure of chromosomes through microscopic analysis.
Cytogenetic testing is the examination of chromosomes to determine chromosome abnormalities such as aneuploidy and structural abnormalities. A normal human cell contains 23 pairs of chromosomes, including 22 pairs of autosomes and a pair of sex chromosomes (XX or XY).
Cytogenetic testing is the examination of chromosomes to determine chromosome abnormalities such as aneuploidy and structural abnormalities. A normal human cell contains 23 pairs of chromosomes, including 22 pairs of autosomes and a pair of sex chromosomes (XX or XY).
Molecular genetics is the study of chromosomes and DNA at the molecular level using DNA technology, whereas cytogenetics is the study of the number and structure of chromosomes through microscopic analysis.
Molecular cytogenetics is a study of genetic disorders using new technologies that combine cytogenetic and molecular techniques (Speicher and Carter, 2005).
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The basic method of molecular cytogenetics is fluorescence in situ hybridization (FISH). It enables a specific detection of unique sequences, chromosomal regions or entire chromosomes in metaphase, interphase cells or in tissue sections.
The Cytogenetics Laboratory is a CLIA-certified and CAP accredited facility that provides comprehensive cytogenetic diagnosis on multiple sample types including peripheral blood, bone marrow, fibroblasts and tissues.
What is molecular diagnostics? Molecular diagnostics, also called molecular pathology, involves taking DNA or RNA, the unique genetic code found in our cells, and analyzing the sequences for red flags that can pinpoint the potential emergence of a specific disease.

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