Back to search

An intragenic deletion of the factor IX gene in a family with hemophilia B.

Data up to Jan 2025

Published1985
Citations47
References17

Total Citations Per Year

Abstract

References (17)

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1975 • 33,059 citations

The Partial Thromboplastin Time with Kaolin: A Simple Screening Test for First Stage Plasma Clotting Factor Deficiencies

1961 • 1,015 citations

Complete nucleotide sequences of the gene for human factor IX (antihemophilic factor B)

1985 • 683 citations

Enzymatic Synthesis of Deoxyribonucleic Acid

1970 • 424 citations

Isolation and characterization of a cDNA coding for human factor IX.

1982 • 415 citations

The gene structure of human anti-haemophilic factor IX.

1984 • 361 citations

Molecular cloning of the gene for human anti-haemophilic factor IX

1982 • 272 citations

Gene deletions in patients with haemophilia B and anti-factor IX antibodies

1983 • 207 citations

Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

1984 • 161 citations

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms

1984 • 145 citations

CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)

1984 • 127 citations

Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.

1983 • 67 citations

CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY)

1984 • 58 citations

Regional localization of the human factor IX gene by molecular hybridization

1983 • 48 citations

Measurement of factor VIII inhibitors.

1984 • 20 citations

Factor IX and prothrombin in amniotic fluid and fetal plasma: constraints on prenatal diagnosis of hemophilia B and evidence of proteolysis

1984 • 14 citations

Factor IX and prothrombin in amniotic fluid and fetal plasma: constraints on prenatal diagnosis of hemophilia B and evidence of proteolysis

1984 • 2 citations

Cited By (0)

Loading...
An intragenic deletion of the factor IX gene in a family with hemophilia B. (1985) – Journal of Clinical Investigation | Metascience Observatory Explorer