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Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders

New sequencing methods capable of rapidly analyzing the genome at increasing resolution have transformed diagnosis of single-gene or oligogenic genetic disorders in pediatric and adult medicine. Targeted tests, consisting of disease-focused multigene panels and diagnostic exome sequencing to interro...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Cold Spring Harb Perspect Med
मुख्य लेखकों: Van den Veyver, Ignatia B., Eng, Christine M.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Cold Spring Harbor Laboratory Press 2015
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC4588135/
https://ncbi.nlm.nih.gov/pubmed/26253094
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a023077
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