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2. An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature. Issue 12 (7th October 2016)

4. Hearing loss in inherited peripheral neuropathies: Molecular diagnosis by NGS in a French series. Issue 9 (8th August 2019)

5. High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5. Issue 1 (4th November 2018)

6. History of tonsillectomy and risk of oropharyngeal cancer. (June 2021)

7. New PRPS1 variant p.(Met68Leu) located in the dimerization area identified in a French CMTX5 patient. Issue 9 (23rd July 2019)