Female haemophilia A in a family with seeming extreme bidirectional lyonization tendency: abnormal premature X-chromosome inactivation?

Author:

Ingerslev Jørgen,Schwartz Marianne,Lamm Lars U.,Kruse Torben A.,Bukh Anne,Stenbjerg Stener

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Prenatal diagnosis of haemophilia A by factor VIII gene analysis;Antonarakis;Lancet,1985a

2. Detection of molecular defects and carriers by DNA analysis;Antonarakis;N. Engl. J. Med.,1985b

3. Molecular genetics of hemophilia A in man;Antonarakis;Mol. Biol. Med.,1987

4. The effect of parental ages on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B;Barrai;Am. J. Hum. Genet.,1968

5. Blood coagulation factor VIII (antihemophilic factor): with comments on von Willebrand's disease and Christmas disease;Barrow;Physiol. Rev.,1974

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