Search

Search Constraints

You searched for: Author/Creator Levy, Jonathan

Search Results

1. 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients. Issue 2 (11th November 2022)

10. Delineation of the clinical profile of CNOT2 haploinsufficiency and overview of the IDNADFS phenotype. Issue 2 (24th November 2022)