Prenatal diagnosis of hereditary amyloidosis in a Portuguese family
- 1 April 1991
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 39 (1) , 123-124
- https://doi.org/10.1002/ajmg.1320390128
Abstract
No abstract availableKeywords
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- Prenatal detection of a gene for hereditary amyloidosisAmerican Journal of Medical Genetics, 1989
- Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy—type I (Portuguese, Andrade)American Journal of Medical Genetics, 1987
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- PRESYMPTOMATIC DIAGNOSIS OF HETEROZYGOSITY FOR FAMILIAL AMYLOIDOTIC POLYNEUROPATHY BY RECOMBINANT DNA TECHNIQUESThe Lancet, 1985
- Polymorphism of human plasma thyroxine binding prealbuminBiochemical and Biophysical Research Communications, 1983