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https://www.verywellfamily.com/parental-karyotype-tests-2371787
A karyotype test can detect deviations from that number, as well as abnormalities in the way each chromosome is formed. In order to obtain a parental karyotype, blood (usually white blood cells) from one or both parents is used.
https://genomicdiagnostics.com.au/our-tests/paediatrics/molecular-karyotype-snp-microarray/
Molecular Karyotype (SNP Microarray) Chromosomal microarray (CMA or Molecular karyotype) is an advanced technique in genetic testing that detects copy number changes in a person’s chromosomes at a much higher resolution than conventional chromosome analysis (karyotype).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839907/
Molecular karyotyping with microarrays and parental support Of the 330 known trisomy 21 cells, 7 were called either monosomy 21 or disomy 21, for a false-negative proportion of 2.1% ( Supplementary Material, Table SII ).Cited by: 300
https://www.fertstert.org/article/S0015-0282(17)30212-1/pdf
The Parental Support algorithm is then used to determine the number and origin of each chromosome. In short, the allele ratios are calculated for each locus across a ... molecular karyotype results or in discordant results from cy-togenetics not explained by technical limitations of the mo-lecular testing methods (i.e., balanced tetraploidy,
https://academic.oup.com/humrep/article/25/4/1066/696985
Jan 24, 2010 · Techniques that use new molecular methods to determine the karyotype of an embryo are expanding the scope of PGS. METHODS We introduce a new method for PGS, termed ‘parental support’, which leverages microarray measurements from parental DNA to ‘clean’ single-cell microarray measurements on embryonic cells and explicitly computes ...Cited by: 300
https://www.sciencedirect.com/science/article/pii/S0015028217302121
Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens. ... The Parental Support algorithm is then used to determine the number and origin of each chromosome. ... In the event of a discordant result between molecular karyotype results or in discordant results from cytogenetics not explained by ...Cited by: 12
https://molecularcytogenetics.biomedcentral.com/articles/10.1186/1755-8166-6-25
Jul 03, 2013 · Molecular mechanisms involved probably are based on the sperm chromosome of paternal origin, which determine the mode of formation. ... Distinct mechanism of formation of the 48, XXYY karyotype. Aránzazu Margallo Balsera 1, ... of the 48,XXYY karyotype to his parents revealed the origin is paternal, as is generally accepted in this syndrome.Cited by: 3
https://www.allelediagnostics.com/services/tests/
Test Menu Our test menu is divided into pediatric and prenatal testing for your convenience. Note that turnaround times listed for all testing are dependent upon specimen quality and quantity received in the laboratory. For information about parental or familial testing, expand the test type associated with the proband’s specimen.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3646811/
Compared with the parental G strain, the most polymorphic bands of clone D11 were bands U (3.05 Mb) and T (2.91 Mb), which were not found in the G strain. These karyotype profiles were reproducible, were obtained repeatedly and proved to be stable in continuous culture of …Cited by: 13
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