about
The phylogeography of Y-chromosome haplogroup h1a1a-m82 reveals the likely Indian origin of the European Romani populationsH1 tau haplotype-related genomic variation at 17q21.3 as an Asian heritage of the European Gypsy populationEXOSC8 mutations alter mRNA metabolism and cause hypomyelination with spinal muscular atrophy and cerebellar hypoplasia.Reconstructing Roma history from genome-wide dataLimitations and plausibility of the Pliocene lignite hypothesis in explaining the etiology of Balkan endemic nephropathyA mutation in an alternative untranslated exon of hexokinase 1 associated with hereditary motor and sensory neuropathy -- Russe (HMSNR).LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population.Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q.Origins, admixture and founder lineages in European Roma.Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2GNE Myopathy: Two Clusters with History and Several Founder Mutations.High prevalence of CYP2C19*2 allele in Roma samples: study on Roma and Hungarian population samples with review of the literature.Refining the South Asian Origin of the Romani people.Transcriptome-wide effects of a POLR3A gene mutation in patients with an unusual phenotype of striatal involvement.Prevalence of URAT1 allelic variants in the Roma population.Carrier rates of four single-gene disorders in Croatian Bayash Roma.UFM1 founder mutation in the Roma population causes recessive variant of H-ABC.Challenges of diagnostic exome sequencing in an inbred founder population.Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.Refining the genetic portrait of Portuguese Roma through X-chromosomal markers.Heritability and genetic correlations of obesity-related phenotypes among Roma people.A genetic historical sketch of European Gypsies: The perspective from autosomal markers.Unique frequencies of HFE gene variants in Roma/Gypsies.ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies.Tau haplotypes support the Asian ancestry of the Roma population settled in the Basque Country.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
A newly discovered founder population: the Roma/Gypsies
@ast
A newly discovered founder population: the Roma/Gypsies
@en
A newly discovered founder population: the Roma/Gypsies
@nl
type
label
A newly discovered founder population: the Roma/Gypsies
@ast
A newly discovered founder population: the Roma/Gypsies
@en
A newly discovered founder population: the Roma/Gypsies
@nl
prefLabel
A newly discovered founder population: the Roma/Gypsies
@ast
A newly discovered founder population: the Roma/Gypsies
@en
A newly discovered founder population: the Roma/Gypsies
@nl
P2093
P356
P1433
P1476
A newly discovered founder population: the Roma/Gypsies
@en
P2093
Luba Kalaydjieva
Raphaelle Chaix
P304
P356
10.1002/BIES.20287
P407
P50
P577
2005-10-01T00:00:00Z