MOSAICISM AND SPORADIC HAEMOPHILIA: IMPLICATIONS FOR CARRIER DETERMINATION
- 4 February 1989
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 333 (8632), 273-274
- https://doi.org/10.1016/s0140-6736(89)91279-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected maleNature, 1987
- Germline mosaicism and Duchenne muscular dystrophy mutationsNature, 1987
- Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophyHuman Genetics, 1987
- Recurrent mutations in haemophilia A give evidence for CpG mutation hotspotsNature, 1986
- Detection and sequence of mutations in the factor VIII gene of haemophiliacsNature, 1985
- Characterization of the human factor VIII geneNature, 1984
- PLASMA ASSAY OF FETAL FACTORS VIIIC AND IX FOR PRENATAL DIAGNOSIS OF HÆMOPHILIAThe Lancet, 1979
- Prenatal Diagnosis of Classic HemophiliaNew England Journal of Medicine, 1979