Molecular basis of the common electrophoretic polymorphism (Fu1/Fu2) in human alpha-L-fucosidase.
Open Access
- 1 August 1994
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 31 (8) , 659-660
- https://doi.org/10.1136/jmg.31.8.659-a
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.Journal of Medical Genetics, 1993
- Huntington's disease: testing the testNature Genetics, 1993
- A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomesMolecular and Cellular Probes, 1993
- A large family with patent ductus arteriosus and unusual face.Journal of Medical Genetics, 1993
- Patent ductus arteriosus in four generations of a family.Journal of Medical Genetics, 1992
- Human α-L-fucosidase: Complete coding sequence form cDNA clonesBiochemical and Biophysical Research Communications, 1989
- Update on counseling the family with a first‐degree relative with a congenital heart defectAmerican Journal of Medical Genetics, 1988
- Familial persistent ductus arteriosus.Archives of Disease in Childhood, 1986
- FAMILIAL PATENT DUCTUS ARTERIOSUSHeart, 1961
- PERSISTENT TRUNCUS ARTERIOSUS IN TWO SIBLINGSHeart, 1961