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Molecular cytogenetic study of short arm aberrations in human D, G group chromosomes.

A study of supernumerary marker chromosomes and Yqs cases suggested that the markers exerted no phenotypic effect, and it was suggested that there might be different mechanisms for the formation of p+ on acrocentric chromosomes.
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[Significance of methylation and abnormal expression of p16 gene in endometrial carcinoma].

P16 gene methylation was an important event in the development of endometrial carcinoma and MSP is an accurate and relatively simple method for evaluating the methylation status of a related gene.
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[Prader-Willi syndrome and genomic imprinting].

MSPCR is a rapid and simple PCR-based assay compared with other cyto-molecular tests and its results were consistent with the clinical diagnosis of PWS, so it seems to be a reliable diagnostic method for PWS patients who show abnormal methylation at SNRPN.
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[Molecular cytogenetic study of an extra small chromosome].

The results showed that this chromosome was from the short arm of chromosome of D/G group, and the origin and genetic effects of this chromosome and fertility of the carriers were also discussed.
PubMed (opens in a new tab)
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