Национальный цифровой ресурс Руконт - межотраслевая электронная библиотека (ЭБС) на базе технологии Контекстум (всего произведений: 634620)
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Российский вестник перинатологии и педиатрии  / №4 2016

CYTOGENETICALLY VISIBLE COPY NUMBER VARIATIONS (CG-CNVS) IN  BANDING AND  MOLECULAR CYTOGENETICS OF  HUMAN; ABOUT HETEROMORPHISMS AND EUCHROMATIC VARIANTS (50,00 руб.)

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Первый авторLiehr
Страниц1
ID562219
АннотацияCopy number variations (CNVs) having no (obvious) clinical effects were rediscovered as major part of human genome in 2004. However, for every cytogeneticist microscopically visible harmless CNVs (CG-CNVs) are well known since decades. Harmless CG-CNVs can be present as heterochromatic or even as euchromatic variants in clinically healthy persons. Here I provide a review on what is known today on the still too little studied harmless human CG-CNVs, point out which can be mixed up with clinically relevant pathological CG-CNVs and shortly discuss that the artificial separation of euchromatic submicroscopic CNVs (MG-CNVs) and euchromatic CG-CNVs is no longer timely. Overall, neither so-called harmless heterochromatic nor so-called harmless euchromatic CG-CNVs are considered enough in evaluation of routine cytogenetic analysis and reporting. This holds especially true when bearing in mind the so-called twohit model suggesting that combination of per se harmless CNVs may lead to clinical aberrations if they are present together in one patient
Liehr, T. CYTOGENETICALLY VISIBLE COPY NUMBER VARIATIONS (CG-CNVS) IN  BANDING AND  MOLECULAR CYTOGENETICS OF  HUMAN; ABOUT HETEROMORPHISMS AND EUCHROMATIC VARIANTS / T. Liehr // Российский вестник перинатологии и педиатрии .— 2016 .— №4 .— С. 184-184 .— URL: https://rucont.ru/efd/562219 (дата обращения: 20.04.2024)

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