R. Jaron

Nasal potential difference in non‐classic cystic fibrosis—long term follow up

E. Picard, H. Blau, E. Kerem, 2008, Pediatric pulmonology.

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection

T. Walsh, M. King, Ming K. Lee, 2016, Neurology.

Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.

M. King, D. Geiger, R. Segel, 2009, American journal of human genetics.

Expanding the phenotype of CRB2 mutations – A new ciliopathy syndrome?

E. Picard, S. Carmi, L. Carmel, 2016, Clinical genetics.

Nasal potential difference in non classic cystic fibrosis – long term follow up

E. Picard, H. Blau, E. Kerem, 2008 .