chromosome

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Researchers from Good Start Genetics, now part of San Francisco, California-based genetic information company Invitae (NYSE: NVTA), are presenting validation data at the American Society for Reproductive Medicine 2017 Scientific Congress and Expo for a novel, NGS-based preimplantation genetic screening technology that accurately identifies certain chromosomal abnormalities potentially missed on other PGS platforms, the company said.
We performed CMA from peripheral blood DNA, using CytoScan[R] Optima Suite (Affymetrix) platform which is SNP array designed for targeting common chromosomal abnormalities.
Keywords: Chromosomal Q-heterochromatin; Alcoholism; Drug addiction
patent 8,921,332 issued on December 30th, 2014, which claims the use of chimeric restriction endonucleases for directing chromosomal gene editing in cells by homologous recombination.
In addition, the frequency of chromosomal aberrations is increased, including chromosome bridges and laggard chromosomes and leads to partition-bundle division (a novel type of chromosomal aberration, in which chromosomes at the transition from anaphase to telophase of mitosis are divided into three, four or six bundles) (Rong et al.
In the Conference, rare diseases including genetic, metabolic and chromosomal disorders in children will be discussed.
To evaluate the pattern of chromosomal imbalances in a child with congenital anomaly.
of heptaplatin significantly reduces the mitotic indices and highly significantly induces chromosomal aberrations (both numerically and structurally) in proliferative bone marrow cells of SWR/J mice.
They will also be able to use chromosomal patterns to determine cancer cells' metastatic potential and drug resistance.
7]) on European, Asian and American populations have shown breast cancer patients to have elevated chromosomal radiosensitivity compared with healthy individuals.
The incidence of chromosomal aberrations in population is approximately 0.
Chromosomal translocations can be formed de novo or can be inherited through so-called 'familial transmission'.
com)-- Screening and diagnosis of chromosomal abnormalities in a foetus has seen a dramatic shift over the last 30 years or so.
Dr Gowri Ramanathan, head of ObGyn and director of Foetal Medicine at Danat Al Emarat Hospital for Women and Children, said screening and diagnosis of chromosomal abnormalities in a foetus has seen a dramatic shift over the past 30 years.
In 2011, Sequenom Laboratories first pioneered the use of noninvasive prenatal testing with the introduction of the MaterniT21 PLUS laboratory-developed test that has helped more than 250,000 pregnant women worldwide who are at a high risk for fetal chromosomal abnormalities.