Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).
about
Human lysosomal acid phosphatase: cloning, expression and chromosomal assignmentIntrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancerContiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeHuman genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probesIndividual exons encode the integral membrane domains of human myelin proteolipid proteinComprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations.Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians.Molecular genetics of the human X chromosome.The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.Comparison of factor IX methylation on human active and inactive X chromosomes: implications for X inactivation and transcription of tissue-specific genes.Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome.Mapping of the mouse X chromosome using random genomic probes and an interspecific mouse crossThe gene structure of human anti-haemophilic factor IX.Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphismsAn intragenic deletion of the factor IX gene in a family with hemophilia B.Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX geneVariations among Japanese of the factor IX gene (F9) detected by PCR-denaturing gradient gel electrophoresis.Linkage mapping of a severe X-linked mental retardation syndrome.The varying frequencies of five DNA polymorphisms of X-linked coagulant factor IX in eight ethnic groups.Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elementsWhy does the human factor IX gene have a G + C content of 40%?Population genetics of coagulant factor IX: frequencies of two DNA polymorphisms in five ethnic groupsGenetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.Monoclonal antibodies to coagulation factor IX define a high-frequency polymorphism by immunoassaysThe evolution of the search for novel genes in mammalian sex determination: from mice to menTightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessmentLinkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms.Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.Single nucleotide primer extension to detect genetic diseases: experimental application to hemophilia B (factor IX) and cystic fibrosis genes.The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.Polymorphism of normal factor IX detected by mouse monoclonal antibodies.The molecular genetics of human monogenic diseases.Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogeny.Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene.Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.Architecture and anatomy of the chromosomal locus in human chromosome 21 encoding the Cu/Zn superoxide dismutase.Are some apparently simple deletions actually two concerted deletions that result from interacting RY(i) hairpin loops?Factor IX gene polymorphisms in Indian population.
P2860
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P2860
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).
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-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
1984年學術文章
@zh-hant
name
Regional localization on the h ...... IX gene (hemophilia B locus).
@ast
Regional localization on the h ...... IX gene (hemophilia B locus).
@en
type
label
Regional localization on the h ...... IX gene (hemophilia B locus).
@ast
Regional localization on the h ...... IX gene (hemophilia B locus).
@en
prefLabel
Regional localization on the h ...... IX gene (hemophilia B locus).
@ast
Regional localization on the h ...... IX gene (hemophilia B locus).
@en
P2093
P2860
P921
P356
P1476
Regional localization on the h ...... r IX gene (hemophilia B locus)
@en
P2093
G Camerino
J L Mandel
J P Lecocq
K H Grzeschik
P Tolstoshev
P2860
P304
P356
10.1073/PNAS.81.2.498
P407
P577
1984-01-01T00:00:00Z