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Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases.
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Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases.
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases. J Med Genet. 2019 12; 56(12):783-791.
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PubMed
subject areas
Child
Exome
Genetic Diseases, Inborn
Genetic Predisposition to Disease
Genome, Human
Humans
Infant
Rare Diseases
Whole Genome Sequencing
authors with profiles
JOHN BELMONT