Number of the records: 1
expanzia trinukleotidových repetícií
Record number d019680 Date 06.06.2025 Type M - MESH Topical term expanzia trinukleotidových repetícií Other term Slovak (Pseudonym) zvýšenie počtu trinukleotidových repetícií
See also (Later heading) fragilita chromozómov
(Later heading) syndróm fragilného chromozómu X
(Later heading) dystrofia myotonická
(Skutočné meno) fragilita chromozómov
(Skutočné meno) syndróm fragilného chromozómu X
(Skutočné meno) dystrofia myotonická
(Skutočné meno) anticipácia genetická
(Skutočné meno) miesta chromozómov fragilné
(Later heading) anticipácia genetická
UDC G02.111.570.080.708.800.140.865G02.111.570.080.708.800.500.850.200G05.360.080.708.800.074.865G05.360.080.708.800.500.850.200G05.360.340.024.189.220.865G05.360.340.024.850.500.850.200G05.365.590.220.865G05.558.220.865 Note An increased number of contiguous trinucleotide repeats in the DNA sequence from one generation to the next. The presence of these regions is associated with diseases such as FRAGILE X SYNDROME and MYOTONIC DYSTROPHY. Some CHROMOSOME FRAGILE SITES are composed of sequences where trinucleotide repeat expansion occurs. 
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Number of the records: 1