Brief research communication: Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with Autism

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 105, Issue 5, 2001, Pages 404-405

  Plank, Sara M ^b   Copeland Yates, Susan A ^a,c   Sossey Alaoui, Khalid ^a   Bell, Jennifer M ^b   Schroer, Richard J ^a   Skinner, Cindy ^a   Michaelis, Ron C ^a  

^a GREENWOOD GENETIC CENTER   (United States)

^b PRESBYTERIAN COLLEGE   (United States)

^c CLEMSON UNIVERSITY   (United States)

Author keywords

Association studies; Autistic disorder; Neurofibromatosis 1 gene

Indexed keywords

ALLELE; ARTICLE; AUTISM; CHILD; CONTROLLED STUDY; FEMALE; GAIT DISORDER; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; NEUROFIBROMATOSIS; NUCLEOTIDE REPEAT; PRIORITY JOURNAL; STEREOTYPY; GENE FREQUENCY; GENETICS; NUCLEOTIDE SEQUENCE; PATHOLOGY; TUMOR SUPPRESSOR GENE;

MICROSATELLITE DNA;

ALLELES; AUTISTIC DISORDER; BASE SEQUENCE; FEMALE; GENE FREQUENCY; GENES, NEUROFIBROMATOSIS 1; HUMANS; INTRONS; MALE; MICROSATELLITE REPEATS;

EID: 0035827825     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.1432     Document Type: Article

References (8)

1. Childhood psychosis and neurofibromatosis: More than just a coincidence?
2. Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) gene
3. Association study of the NF1 gene and autistic disorder
4. Lack of independence between five DNA polymorphisms in the NF1 gene
5. Von recklinghaus neurofibromatosis
6. Linkage disequilibrium between four intragenic polymorphic microsatellites of the NF1 gene and its implications for genetic counselling
7. The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type I gene
8. An Alu polymorphism intragenic to the neurofibromatosis type 1 gene (NF1)