De novo deletions of the 5q13 region and prenatal diagnosis of spinal muscular atrophy
- 1 January 1995
- journal article
- letter
- Published by Wiley in Prenatal Diagnosis
- Vol. 15 (1) , 93-94
- https://doi.org/10.1002/pd.1970150121
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.Journal of Medical Genetics, 1992
- Prenatal prediction of spinal muscular atrophy.Journal of Medical Genetics, 1992
- Mapping of acute (type I) spinal muscular atrophy to chromosome 5q12-q14The Lancet, 1990
- Genetic homogeneity between acute and chronic forms of spinal muscular atrophyNature, 1990
- Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3Nature, 1990