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The Molecular Basis of Severe Hemophilia B in a Girl

Data up to Jan 2025

Published1986
Citations46
References25

Total Citations Per Year

Abstract

References (25)

A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES

1971 • 5,049 citations

The gene structure of human anti-haemophilic factor IX.

1984 • 361 citations

Human N-myc is closely related in organization and nucleotide sequence to c-myc

1986 • 273 citations

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

1982 • 272 citations

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

1985 • 231 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

Human chromosomes structure, behavior, effects

1982 • 121 citations

Cytologic evidence for three human X-chromosomal segments escaping inactivation

1983 • 108 citations

Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene.

1984 • 86 citations

Severe factor VIII and factor IX deficiency in females

1978 • 84 citations

X chromosome constitution and the human female phenotype

1980 • 79 citations

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

1984 • 58 citations

Human Chromosomes

1980 • 34 citations

DNA replication and inactivation patterns in structural abnormality of sex chromosomes

1984 • 33 citations

Variant of Factor IX Deficiency in Female with 45, X Turner’s Syndrome

1970 • 30 citations

The molecular genetics of hemophilia: Blood clotting factors VIII and IX

1985 • 29 citations

The Occurrence of Homozygous Hemophilia in the Female

1971 • 23 citations

Christmas Disease (Haemophilia B) in a Girl with Deletion of the Short Arm of One X‐Chromosome (Functional Turner Syndrome)

1976 • 22 citations

Christmas Disease in a Girl

1969 • 18 citations

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes

1986 • 14 citations

Pregnancy and delivery in a woman with hemophilia B.

1975 • 12 citations

More precise localization of the human Factor IX gene by in situ hybridization

1985 • 10 citations

Current Concepts in the Management of Hemophilia

1985 • 5 citations

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The Molecular Basis of Severe Hemophilia B in a Girl (1986) – New England Journal of Medicine | Metascience Observatory Explorer