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Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

Data up to Jan 2025

Published1985
Citations231
References15

Total Citations Per Year

Abstract

References (15)

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

Characterization of the human factor VIII gene

1984 • 983 citations

Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

1981 • 910 citations

Expression of active human factor VIII from recombinant DNA clones

1984 • 699 citations

Construction of linkage maps with DNA markers for human chromosomes

1985 • 325 citations

DIRECT GENE ANALYSIS OF CHORIONIC VILLI: A POSSIBLE TECHNIQUE FOR FIRST-TRIMESTER ANTENATAL DIAGNOSIS OF HAEMOGLOBINOPATHIES

1981 • 189 citations

Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

1984 • 178 citations

DNA restriction fragment length polymorphisms and heterozygosity in the human genome

1984 • 147 citations

A three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.

1983 • 122 citations

A CLINICALLY USEFUL DNA PROBE CLOSELY LINKED TO HAEMOPHILIA A

1984 • 110 citations

PLASMA ASSAY OF FETAL FACTORS VIIIC AND IX FOR PRENATAL DIAGNOSIS OF HÆMOPHILIA

1979 • 99 citations

Amounts, synthesis, and some properties of intracisternal A particle-related RNA in early mouse embryos.

1984 • 89 citations

Genetic Metabolic Disease

1980 • 66 citations

Genotype Assignment (Carrier Detection) in the Haemophilias

1979 • 49 citations

Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.

1984 • 19 citations

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Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in… (1985) – Nature | Metascience Observatory Explorer