Paediatric Haematology Research Unit
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- 1993
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Mark
Piebaldism in a mentally retarded girl with rare deletion of the long arm of chromosome 4
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- Contribution to journal › Article
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Mark
HIV infection in haemophilia - A European cohort
(
- Contribution to journal › Article
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Mark
Report of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosis
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- Contribution to journal › Article
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Mark
Haemophilia : strategies for carrier detection and prenatal diagnosis
(
- Contribution to journal › Article
- 1992
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Mark
Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden
(
- Contribution to journal › Article
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Mark
Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion
(
- Contribution to journal › Article
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Mark
Factor VIII and factor IX inhibitors in haemophiliacs
(
- Contribution to journal › Letter
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Mark
Gaucher's disease in an infant diagnosed by fine needle aspiration of the liver and spleen : A case report
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- Contribution to journal › Article
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Mark
Haplotype analysis of identical factor IX mutants using PCR
(
- Contribution to journal › Article
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Mark
Further characterization of the new marker at DXS115 with regard to carrier detection in hemophilia A
(
- Contribution to journal › Letter