A clinically useful DNA probe closely linked to haemophilia A.
about
The European Hematology Association Roadmap for European Hematology Research: a consensus documentSex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysisFetal tissue sampling. The San Francisco experience with 190 pregnancies.A computer programme to calculate risk in X linked disorders using multiple marker loci.Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphismFirst trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13.Nonrandom X chromosome DNA methylation patterns in hemophiliac females.X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studiesA contiguous, 3-Mb physical map of Xq28 extending from the colorblindness locus to DXS15.Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.Nonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides.Identification of carriers of haemophilia by polymerase chain reaction.The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.More than half the sporadic cases of hemophilia A in Sweden are due to a recent mutation.Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene.Factor VIII gene polymorphisms in the Asian Indian population.Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A.Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP).Evaluation of DNA-based diagnosis for haemophilia A.A recurrent missense mutation (Arg----Gln) and a partial deletion in factor VIII gene causing severe haemophilia A.Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms.Current strategy for genetic analysis of haemophilia A families.Polymorphisms associated with the FVIII and FIX genes in the Turkish population.
P2860
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P2860
A clinically useful DNA probe closely linked to haemophilia A.
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
A clinically useful DNA probe closely linked to haemophilia A.
@en
A clinically useful DNA probe closely linked to haemophilia A.
@nl
type
label
A clinically useful DNA probe closely linked to haemophilia A.
@en
A clinically useful DNA probe closely linked to haemophilia A.
@nl
prefLabel
A clinically useful DNA probe closely linked to haemophilia A.
@en
A clinically useful DNA probe closely linked to haemophilia A.
@nl
P2093
P1433
P1476
A clinically useful DNA probe closely linked to haemophilia A.
@en
P2093
E G Tuddenham
K E Davies
M E Pembrey
R M Winter
P356
10.1016/S0140-6736(84)91995-0
P407
P577
1984-07-01T00:00:00Z