Medicine
 |
|
18 october 2017 16:39:03 |
| Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases (BMC Medical Genetics) |
|
Tweet Omphalocele is a congenital midline ventral body wall defect that can exist as isolated malformation or as part of a syndrome. It can be considered one of the major and most frequent clinical manifestation of ... |
| 92 viewsCategory: Genetics, Medicine |
 Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients (BMC Medical Genetics)Effects of herpes simplex virus vectors encoding poreless TRPV1 or protein phosphatase 1? in a rat cystitis model induced by hydrogen peroxide (Gene Therapy) 
|
| blog comments powered by Disqus |
MyJournals.org
The latest issues of all your favorite science journals on one page
The latest issues of all your favorite science journals on one page
