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Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.
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Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. PLoS One. 2010 Mar 05; 5(3):e9476.
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PubMed
subject areas
Fragile X Mental Retardation Protein
Fragile X Syndrome
Gene Deletion
Humans
Male
Mutation
Mutation, Missense
Oligonucleotide Array Sequence Analysis
Phenotype
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Sequence Analysis, DNA
Trinucleotide Repeat Expansion
authors with profiles
Elizabeth Berry-Kravis