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Home > For Clinicians > List Of Publications > Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report

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Preimplantation genetic testing legislation and accessibility in the Nordic countries

Whole-genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome

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