Objective: 3p deletion syndrome is a rare monosomal disease that encompasses deletions throughout the short arm of chromosome 3. It is often in the distal region (3p25-pter), but variations in ...
As part of our ongoing commitment to Dixon and the surrounding communities, we continue to expand the services available at CGH’s Dixon Medical Center. Located at 1321 N. Galena Avenue, the Dixon ...
Abstract: Array based comparative genomic hybridization (CGH) is a molecular cytogenetic method for the detection of chromosomal imbalances and it has been extensively used for studying copy number ...
1 Genetic Laboratory AbaCid, HM Hospitales, Hospital Universitario HM Sanchinarro, Madrid, Spain 2 EGOM (Equipo Médico de Ginecología y Obstetricia), HM Hospitales, Madrid, Spain Currently, there is a ...
DUBLIN--(BUSINESS WIRE)--The "Molecular Cytogenetics - Global Strategic Business Report" report has been added to ResearchAndMarkets.com's offering. Global Molecular Cytogenetics Market to Reach $3.5 ...
Variants in the DMD gene, that encodes the cytoskeletal protein, dystrophin, cause a severe form of dilated cardiomyopathy (DCM) associated with high rates of heart failure, heart transplantation, and ...
SANTA CLARA, Calif.--(BUSINESS WIRE)--Agilent Technologies Inc. (NYSE:A) today announced that scientists using the company’s comparative genomic hybridization (CGH) technology have shown that cancer ...
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