Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
about
Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complexTwo progenitor cells for human oogonia inferred from pedigree data and the X-inactivation imprinting model of the fragile-X syndromePhysical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.Mapping the human alpha globin gene complex to 16p13.2----pterLocalization of the mcf.2 transforming sequence to the X chromosome.Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardationCharacterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).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 effectEfficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesLinkage studies in a large fragile X family.Fragile X syndrome: molecular analysis reveals a new mechanism of mutation in human genetic diseases.Use of DNA probes for diagnosis and prevention of inherited disorders.An estimating function approach to linkage heterogeneity.Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.
P2860
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P2860
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@ast
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@en
type
label
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@ast
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@en
prefLabel
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@ast
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@en
P2093
P2860
P356
P1476
Genetic analysis of the fragil ...... nking polymorphic DNA markers.
@en
P2093
Froster-Iskenius U
Kloepfer C
P2860
P304
P356
10.1073/PNAS.83.4.1016
P407
P50
P577
1986-02-01T00:00:00Z