A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23a
Open Access
- 1 April 1991
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 615 (1) , 306-315
- https://doi.org/10.1111/j.1749-6632.1991.tb37772.x
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Genetic heterogeneity in tuberous sclerosisGenomics, 1990
- Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23Genomics, 1990
- Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.Proceedings of the National Academy of Sciences, 1990
- Absence of linkage of ABO blood group locus to familial tuberous sclerosisExperimental Neurology, 1989
- Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17Experimental Neurology, 1989
- Heterogeneity evidence and linkage studies on Charcot‐Marie‐Tooth diseaseNeurology, 1989
- TUBEROUS SCLEROSIS AND ABOThe Lancet, 1987
- LINKAGE OF TUBEROUS SCLEROSIS TO ABO BLOOD GROUPThe Lancet, 1987
- FIRST TRIMESTER PRENATAL EXCLUSION OF TUBEROUS SCLEROSISThe Lancet, 1987
- EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9Published by Elsevier ,1987