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12. Expanding the molecular diversity and phenotypic spectrum of glycerol 3‐phosphate dehydrogenase 1 deficiency. Issue 5 (1st July 2016)

15. Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN. Issue 6 (14th April 2011)

16. Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia. Issue 2 (15th November 2019)

18. Positioning Europe for the EPITRANSCRIPTOMICS challenge. Issue 6 (3rd June 2018)