Genetics
 |
|
14 december 2018 12:00:04 |
| Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants (European Journal of Human Genetics) |
|
Tweet |
| 76 viewsCategory: Genetics |
 A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencing (European Journal of Human Genetics)The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study (European Journal of Human Genetics) 
|
| 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
