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TKG
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Author Details
Full Name
Tena Varvil
Affiliation
ORCID
Career Start Year
1993
Papers
12
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
24467814
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.
Mol Autism
2014
23341896
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
PLoS One
2013
19455147
Genome-wide linkage in Utah autism pedigrees.
Mol Psychiatry
2010
11204593
Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.
Thromb Haemost
2001
10726711
Evaluation of heterodimeric guanylyl cyclase genes as candidates for human hypertension.
J Hypertens
2000
10514109
A locus for febrile seizures (FEB3) maps to chromosome 2q23-24.
Ann Neurol
1999
8652836
Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2.
Blood
1996
8659518
Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q.
Am J Hum Genet
1996
7825577
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
Am J Hum Genet
1995
8001971
Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36.
Genomics
1994
7874147
Dinucleotide repeat polymorphism from a cosmid containing the human anion exchanger isoform 3 (SLC2C) gene.
Hum Mol Genet
1994
7683738
Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein gene.
Lancet
1993
1 - 12 of 12
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