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Orvosi Hetilap|February 12, 1998
[Androgen receptor gene (CAG)n of spinal and bulbar muscular atrophy found in the normal child population in Hungary]J Molnár, A Kis, B MeleghOrvosi Hetilap|August 14, 1998
[Diagnosis of Prader-Willi syndrome by reverse transcriptase polymerase chain reaction]T Varjas, E Nádasi, E Kovács, et al.Orvosi Hetilap|June 3, 1998
[Mutation analysis in the CTG-base multiplication in a family with myotonic dystrophy in three generations]J Molnár, A Kis, B Melegh, et al.American Journal of Medical Genetics|November 24, 1999
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian populationP Gyürüs, J Molnár, B Melegh, et al.Orvosi Hetilap|June 5, 1998
[Incidence of factor V G1681A (Leiden) mutation in samplings from the Hungarian population]J Stankovics, B Melegh, A Nagy, et al.Acta Biologica Hungarica|January 1, 1997
Phosphofructokinase interacts with molecular chaperonins GroEL and GroESB Melegh, Y MinamiActa Paediatrica Hungarica|January 1, 1991
Carnitine content of red blood cells of human subjects treated with pivampicillin and carnitineB Melegh, V JászaiNeuropediatrics|December 31, 1997
Valproate treatment induces lipid globule accumulation with ultrastructural abnormalities of mitochondria in skeletal muscleB Melegh, K TrombitásCurrent Medicinal Chemistry|September 15, 2009
Functional variants of the interleukin-23 receptor gene in non-gastrointestinal autoimmune diseasesE Safrany, B MeleghPageof 31