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Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
Ali Jalali
, Kimberly A. Aldinger
, Ajit Chary
, David G. Mclone
, Robin M. Bowman
, Luan Cong Le
, Phillip Jardine
, Ruth Newbury-Ecob
, Andrew Mallick
, Nadereh Jafari
, Eric J. Russell
, John Curran
, Pam Nguyen
, Karim Ouahchi
, Charles Lee
,
William B. Dobyns
, Kathleen J. Millen
, Joao M. Pina-Neto
, John A. Kessler
, Alexander G. Bassuk
Research output
:
Contribution to journal
›
Article
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peer-review
34
Scopus citations
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Dive into the research topics of 'Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity'. Together they form a unique fingerprint.
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Keyphrases
Genetic Heterogeneity
100%
Autosomal Dominant
100%
Cephalocele
100%
Dandy-Walker Malformation
100%
Vietnamese Americans
37%
American Family
25%
Pedigree
25%
Brazil
12%
Chromosomal Region
12%
Neuroimaging Studies
12%
Multipoint
12%
Haplotype Analysis
12%
Chromosome 2
12%
Linkage Analysis
12%
LOD Score
12%
Terminal Deletion
12%
Genome-wide Linkage Analysis
12%
Genetic Etiology
12%
Locus Heterogeneity
12%
Biochemistry, Genetics and Molecular Biology
Genetic Heterogeneity
100%
Autosomal Dominant Inheritance
100%
Gene Linkage
100%
Linkage Analysis
25%
Pedigree
25%
Genetics
12%
Haplotype
12%
Chromosome 2
12%