Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission
about
Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disordersPrenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.Numerous length polymorphisms at short tandem repeats in human cytomegalovirus.Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expressionEMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders
P2860
Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Decrease in the CGGn trinucleo ...... e during paternal transmission
@ast
Decrease in the CGGn trinucleo ...... e during paternal transmission
@en
type
label
Decrease in the CGGn trinucleo ...... e during paternal transmission
@ast
Decrease in the CGGn trinucleo ...... e during paternal transmission
@en
prefLabel
Decrease in the CGGn trinucleo ...... e during paternal transmission
@ast
Decrease in the CGGn trinucleo ...... e during paternal transmission
@en
P2093
P2860
P1476
Decrease in the CGGn trinucleo ...... e during paternal transmission
@en
P2093
P2860
P304
P407
P577
1996-09-01T00:00:00Z