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Search Results - Cazón‐Varela, Laura
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Deletions of specific exons of FHOD3 detected by next‐generation sequencing are associated with hypertrophic cardiomyopathy
by
Ochoa, Juan P.
,
Lopes, Luis R.
,
Perez‐Barbeito, Marlene
,
Cazón‐Varela, Laura
,
Torre‐Carpente, Maria M.
,
Sonicheva‐Paterson, Natalia
,
De Uña‐Iglesias, David
,
Quinn, Ellen
,
Kuzmina‐Krutetskaya, Svetlana
,
Garrote, José A.
,
Elliott, Perry M.
,
Monserrat, Lorenzo
Published in
Clinical genetics
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Clinical Genetics
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Cardiomyopathies
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Cardiomyopathy
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Dna Copy-Number Variations
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Dna Copy‐Number Variations
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Exons
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Fhod3 Protein
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Formins
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Genetic Analysis
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Genetic Testing
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Genetics & Heredity
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Genomes
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Human
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Hypertrophic
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Life Sciences & Biomedicine
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Next-Generation Sequencing
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Next‐Generation Sequencing
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