DNA from guthrie spots for diagnosis of DMD by multiplex PCR
- 31 December 1990
- journal article
- other
- Published by Elsevier BV in Biochemical Medicine and Metabolic Biology
- Vol. 44 (3), 294-295
- https://doi.org/10.1016/0885-4505(90)90075-c
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- RAPID DETECTION OF βs DNA FROM GUTHRIE CARDS BY CHROMOGENIC PROBESThe Lancet, 1989
- Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophiesNeurology, 1989
- Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningHuman Genetics, 1989
- GUTHRIE SPOTS FOR DNA-BASED CARRIER TESTING IN CYSTIC FIBROSISThe Lancet, 1988
- Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplificationNucleic Acids Research, 1988
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screeningHuman Genetics, 1987