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1.
Brief report: high-throughput sequencing of IL23R reveals a low-frequency, nonsynonymous single-nucleotide polymorphism that is associated with ankylosing spondylitis in a Han Chinese population.
Arthritis Rheum
; 65(7): 1747-52, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23606107
2.
Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia.
PLoS Genet
; 7(3): e1002027, 2011 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-21455487
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