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- 2022
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Mark
Dominantly inherited myosin IIa myopathy caused by aberrant splicing of MYH2
(
- Contribution to journal › Article
- 2016
-
Mark
Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa
(
- Contribution to journal › Article
- 1994
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Mark
Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III
(
- Contribution to journal › Article
-
Mark
Serum thymidine kinase in congenital dyserythropoietic anaemia type III
(
- Contribution to journal › Article
- 1993
-
Mark
Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type III
(
- Contribution to journal › Article