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3. Brain calcifications and PCDH12 variants. (August 2017)

4. Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy. Issue 8 (28th July 2021)

7. Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection. (24th May 2016)

9. Mitochondrial PITRM1 peptidase loss-of-function in childhood cerebellar atrophy. Issue 9 (15th May 2018)