Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reaction
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference6 articles.
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2. Newborn factor VIII complex: elevated activities in term infants and alterations in electrophoretic mobility related to illness and activated coagulation;Johnson;Br J Haematol,1981
3. Cloning and characterisation of two cDNAs coding for human von Willebrand factor;Sadler;Proc Natl Acad Sci USA,1985
4. Construction of cDNA coding for human von Willebrand factor using antibody probes for colony-screening and mapping of the chromosomal gene;Verweij;Nucleic Acids Res,1985
5. Ir Peake, D. Bowen, P. Bignell, et al., Family studies and prenatal diagnosis in severe von Willebrand's disease by polymerase chain reaction amplification of a variable number tandem repeat (VNTR) region of the von Willebrand factor gene, Blood ((in press)).
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1. Von Willebrand Factor 1 and Factor 2 Alleles (Intron 40) Are Suitable Markers for Carrier Detection in von Willebrand Disease Families in the Indian Population;Acta Haematologica;2006
2. Hemostatic abnormalities;Neonatal Hematology;2005-08-18
3. Hemostatic Disorders of the Newborn;Avery's Diseases of the Newborn;2005
4. The molecular biology of von Willebrand disease;Clinical & Laboratory Haematology;2001-08-01
5. Von willebrand disease and quantitative variation in von willebrand factor;Journal of Laboratory and Clinical Medicine;1997-09
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