Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome.
about
A novel mutation in the invariant AG of the acceptor splice site of intron 4 of the beta-hexosaminidase alpha-subunit gene in two unrelated American black GM2-gangliosidosis (Tay-Sachs disease) patients1(st) trimester miscarriage: four decades of studyA case of apparent trisomy 21 without the Down's syndrome phenotype.Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, IrelandMaternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.Normal phenotype with paternal uniparental isodisomy for chromosome 21.Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangementsComparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.DNA polymorphism analysis in families with recurrence of free trisomy 21.Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternalThe meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis.Cytogenetic study in children with down syndrome among kosova Albanian population between 2000 and 2010.Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS).Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21.
P2860
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P2860
Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome.
description
1991 nî lūn-bûn
@nan
1991 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@ast
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@en
type
label
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@ast
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@en
prefLabel
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@ast
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@en
P2093
P2860
P1476
Use of short sequence repeat D ...... hromosome 21 in Down syndrome.
@en
P2093
Antonarakis SE
Collins FA
Economou EP
Mikkelsen M
Petersen MB
Schinzel AA
Tranebjaerg L
P2860
P407
P577
1991-01-01T00:00:00Z