Pages that link to "Q45886034"

The following pages link to Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene (Q45886034):

Displaying 50 items.

• hemophilia (Q134003) (← links)
• Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16 (Q24624142) (← links)
• Genetic analysis of haemophilia A in Bulgaria (Q24805057) (← links)
• In search of the eighth factor: a personal reminiscence (Q28188221) (← links)
• Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians (Q33596659) (← links)
• Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis (Q33597606) (← links)
• X linked neonatal centronuclear/myotubular myopathy: evidence for linkage to Xq28 DNA marker loci (Q33597660) (← links)
• Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene (Q33674055) (← links)
• Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism (Q33838180) (← links)
• Haemophilia A and haemophilia B: molecular insights (Q33918888) (← links)
• Rapid screening of a human genomic library in yeast artificial chromosomes for single-copy sequences (Q34294624) (← links)
• Molecular etiology of factor VIII deficiency in hemophilia A. (Q34309231) (← links)
• Detection of specific DNA sequences by fluorescence amplification: a color complementation assay (Q34322232) (← links)
• A chromosome 11-linked determinant controls fetal globin expression and the fetal-to-adult globin switch (Q34366910) (← links)
• First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13. (Q34487918) (← links)
• Nonrandom X chromosome DNA methylation patterns in hemophiliac females (Q34571270) (← links)
• Complementary strand analysis: a new approach for allelic separation in complex polyallelic genetic systems. (Q34630029) (← links)
• The molecular basis of hemophilia A. (Q34886372) (← links)
• A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia A. (Q35044169) (← links)
• Detection of DNA sequence polymorphisms in human genomic DNA by using denaturing gradient gel blots (Q35195096) (← links)
• Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304). (Q35197242) (← links)
• A homozygous transthyretin variant associated with senile systemic amyloidosis: evidence for a late-onset disease of genetic etiology (Q35198180) (← links)
• The X chromosome shows less genetic variation at restriction sites than the autosomes (Q35198721) (← links)
• Nonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides (Q35245535) (← links)
• Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq. (Q35246514) (← links)
• Maternal duplication associated with gene deletion in sporadic hemophilia (Q35246850) (← links)
• Application of DNA-DNA hybridization of dual labeled probes to the detection of trisomy 21, monosomy 21, and sex determination (Q35247507) (← links)
• Preimplantation single-cell analysis of multiple genetic loci by whole-genome amplification (Q35558984) (← links)
• A TaqI polymorphism adjacent to the factor VIII gene (F8C). (Q35805912) (← links)
• Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor gene (Q35811246) (← links)
• Recently recognized chromosomal defects of clinical importance (Q36706952) (← links)
• Identification of carriers of haemophilia by polymerase chain reaction. (Q36751871) (← links)
• The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B (Q36775668) (← links)
• Rapid assessment of haemophilia A carrier state by non-invasive techniques using the polymerase chain reaction (Q37259553) (← links)
• Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene (Q37582874) (← links)
• Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresis (Q37596425) (← links)
• Mutations and a polymorphism in the factor VIII gene discovered by denaturing gradient gel electrophoresis (Q37717801) (← links)
• Clinical advances in hemophilia management (Q37900933) (← links)
• Factor VIII and haemophilia A. (Q38240538) (← links)
• Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria (Q39289662) (← links)
• Polymorphic DNA markers genetically linked to disease-causing genes: a review (Q39461695) (← links)
• Diagnosis of genetic disease using recombinant DNA. (Q39502026) (← links)
• The physiology and pathophysiology of the factor VIII complex (Q39591751) (← links)
• Molecular pathology and immunology of factor VIII (hemophilia A and factor VIII inhibitors). (Q39592850) (← links)
• The impact of DNA analysis on fetal diagnosis (Q39693617) (← links)
• Application of DNA-based diagnosis to patient care: the example of hemophilia A. (Q39765333) (← links)
• The use of filter-bound DNA fragments as templates for radiolabelling by random priming (Q40448694) (← links)
• The hemophilias. (Q40519633) (← links)
• Rapid Polymerase Chain Reaction Analysis of St14 (DXS52) VNTR: Carrier Detection of Hemophilia A (Q40884820) (← links)
• Somatic origin of inherited haemophilia A. (Q41187736) (← links)