The genetics of rett syndrome: The consequences of a disorder where every case is a new mutation
- 1 January 1986
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 25 (S1), 383-388
- https://doi.org/10.1002/ajmg.1320250540
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Assignment of the Gene for Myelin Proteolipid Protein to the X Chromosome: Implications for X-Linked Myelin DisordersScience, 1985
- The Genetic Linkage Map of the Human X ChromosomeScience, 1985
- The clinical pattern of the rett syndromeBrain & Development, 1985
- Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresisCell, 1984