Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism
- 1 June 2001
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 105 (5) , 404-405
- https://doi.org/10.1002/ajmg.1432
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Association study of the NF1 gene and autistic disorderAmerican Journal of Medical Genetics, 1999
- Linkage disequilibrium between four intragenic polymorphic microsatellites of the NF1 gene and its implications for genetic counselling.Journal of Medical Genetics, 1996
- Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) geneHuman Molecular Genetics, 1993
- Lack of independence between five DNA polymorphisms in the NF1 geneHuman Molecular Genetics, 1993
- The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene.Molecular and Cellular Biology, 1991
- An Alu polymorphism intragenic to the neurofibromatosis type 1 gene (NF1)Nucleic Acids Research, 1991
- Childhood psychosis and neurofibromatosis—more than a coincidence?Journal of Autism and Developmental Disorders, 1984
- Von Recklinghausen NeurofibromatosisNew England Journal of Medicine, 1981