Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

BACKGROUND: Pediatric disorders include a range of highly genetically heterogeneous conditions amenable to genome-wide diagnostic approaches. Finding a molecular diagnosis is challenging but can have profound lifelong benefits. METHODS: The Deciphering Developmental Disorders (DDD) study recruited &...

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Bibliografiset tiedot
Julkaisussa:N Engl J Med
Päätekijät: Wright, Caroline F., Campbell, Patrick, Eberhardt, Ruth Y., Aitken, Stuart, Perrett, Daniel, Brent, Simon, Danecek, Petr, Gardner, Eugene J., Chundru, V. Kartik, Lindsay, Sarah J., Andrews, Katrina, Hampstead, Juliet, Kaplanis, Joanna, Samocha, Kaitlin E., Middleton, Anna, Foreman, Julia, Hobson, Rachel J., Parker, Michael J., Martin, Hilary C., FitzPatrick, David R., Hurles, Matthew E., Firth, Helen V.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2023
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7614484/
https://ncbi.nlm.nih.gov/pubmed/37043637
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1056/NEJMoa2209046.
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