The marker (X) syndrome: a cytogenetic and genetic analysis.
about
A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility.Simple tandem DNA repeats and human genetic diseaseThe unstable repeats--three evolving faces of neurological diseaseStudy of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 GeneProgress toward therapeutic potential for AFQ056 in Fragile X syndrome.The fragile X: progress toward solving the puzzleTwo progenitor cells for human oogonia inferred from pedigree data and the X-inactivation imprinting model of the fragile-X syndromeMolecular and cellular genetics of fragile X syndrome.Molecular cloning and analysis of the fragile X region in manIsolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.Fragile X testing in a diagnostic cytogenetics laboratory.Genotype prediction in the fragile X syndrome.Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligenceA community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology.The frequency of the fragile X chromosome among schoolchildren in CoventryTwelve families with fragile X(q27)Replication status of fragile X(q27.3) in 13 female heterozygotes.Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.Research strategies in human behaviour genetics.Clinical features and reproductive patterns in fragile X female heterozygotes.Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats.X inactivation of the FMR1 fragile X mental retardation geneRole of maternal gesture use in speech use by children with fragile X syndrome.DNA testing for fragile X syndrome in schools for learning difficulties.Neurobehavioral effects of the fragile X premutation in adult women: a controlled study.Fragile-X syndrome: unique genetics of the heritable unstable elementA microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome.Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).Population genetic consequences of the fragile-X syndrome, based on the X-inactivation imprinting model.Methylation status of genes flanking the fragile site in males with the fragile-X syndrome: a test of the imprinting hypothesis.Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectGenetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.Unaffected carrier males in families with fragile X syndrome.A common fragile site at Xq27: theoretical and practical implications.Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.Population dynamics of a meiotic/mitotic expansion model for the fragile X syndromeThe fragile X premutation in carriers and its effect on mutation size in offspringFragile X syndrome: molecular analysis reveals a new mechanism of mutation in human genetic diseases.Molecular heterogeneity of the fragile X syndrome.
P2860
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P2860
The marker (X) syndrome: a cytogenetic and genetic analysis.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年学术文章
@wuu
1984年学术文章
@zh
1984年学术文章
@zh-cn
1984年学术文章
@zh-hans
1984年学术文章
@zh-my
1984年学术文章
@zh-sg
1984年學術文章
@yue
1984年學術文章
@zh-hant
name
The marker (X) syndrome: a cytogenetic and genetic analysis.
@en
The marker
@nl
type
label
The marker (X) syndrome: a cytogenetic and genetic analysis.
@en
The marker
@nl
prefLabel
The marker (X) syndrome: a cytogenetic and genetic analysis.
@en
The marker
@nl
P2093
P2860
P1476
The marker (X) syndrome: a cytogenetic and genetic analysis.
@en
P2093
P2860
P356
10.1111/J.1469-1809.1984.TB00830.X
P407
P577
1984-01-01T00:00:00Z