Filter your results
- 2
- 1
- 2
- 1
- 3
- 2
- 1
- 2
- 1
- 1
- 1
- 1
- 3
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
|
|
sorted by
|
|
Heterogeneous clinical features in Cockayne syndrome-A patients with the same mutation and in siblings2022
Preprints, Working Papers, ...
pasteur-03548783v1
|
||
|
Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndromeMOLECULAR GENETICS & GENOMIC MEDICINE, 2022, 10 (7), ⟨10.1002/mgg3.1954⟩
Journal articles
hal-03780229v1
|
||
Importance comparative respective de l'analyse infra rouge et de l'analyse chimique classique dans le diagnostique étiologique de la lithiase urinaireTunisie Medicale, 1998, 76 (2), pp.1056-1060
Journal articles
pasteur-01985701v1
|