Diagnostic value of exome and whole genome sequencing in craniosynostosis

BACKGROUND: Craniosynostosis, the premature fusion of one or more cranial sutures, occurs in ∼1 in 2250 births, either in isolation or as part of a syndrome. Mutations in at least 57 genes have been associated with craniosynostosis, but only a minority of these are included in routine laboratory gen...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Med Genet
मुख्य लेखकों: Miller, Kerry A, Twigg, Stephen R F, McGowan, Simon J, Phipps, Julie M, Fenwick, Aimée L, Johnson, David, Wall, Steven A, Noons, Peter, Rees, Katie E M, Tidey, Elizabeth A, Craft, Judith, Taylor, John, Taylor, Jenny C, Goos, Jacqueline A C, Swagemakers, Sigrid M A, Mathijssen, Irene M J, van der Spek, Peter J, Lord, Helen, Lester, Tracy, Abid, Noina, Cilliers, Deirdre, Hurst, Jane A, Morton, Jenny E V, Sweeney, Elizabeth, Weber, Astrid, Wilson, Louise C, Wilkie, Andrew O M
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BMJ Publishing Group 2017
विषय:
Developmental Defects
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC5366069/
https://ncbi.nlm.nih.gov/pubmed/27884935
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2016-104215
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