Broschiertes Buch
Assessment of Genetics Mutations,PEX1,PEX2, PEX3,PEX5,PEX6,PEX10,PEX12,PEX13,PEX14,PEX16, PEX19,PEX26 Zellweger syndrome
10. Dezember 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetic Mutations in Genes DSM-IV, DRD4, SERT, HTR1B, SNAP25, GRIN2A, ADRA2A, TPH2, BDNF, induced ADHD
2. November 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of the chronic myeloproliferative disorders in patients with CML mutations Philadelphia chromosome BCR/ABL1
26. Oktober 2016
LAP Lambert Academic Publishing
Ähnliche Artikel
Broschiertes Buch
Assessment of Genes Mutations HLA-DQB1,HLA-DR2,HLA-DR14, In patients with sleep disorders and insomnia Family
31. Oktober 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetics Mutation NOTCH3 Gene in Patients with Migraine Disease
11. November 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetics Mutation Gene HPRT1 in induce Lesch-Nyhan Disease
10. November 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetics Mutations in RNF213, ACTA2, GUCY1A3 Genes induction Moyamoya disease
10. Dezember 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetic Mutations in Parkinson's disease (PD)
4. November 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetics Mutation PRNP Gene induction Prion disease in Human
2. Dezember 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Genetic Evaluation Mutations in the Genes 5-HTTLPR and SLC6A4 and SCC6A4 in the Loyalty to Love or Betrayal of Love
7. November 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Genetics Mutations DCDC2,KIAA0319,DYX1C1 Genes induction Dyslexia disease
18. November 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Mutation Genetics in HTT (High Repetition-CAG), Gene for induced Huntington's disease
7. November 2016
LAP Lambert Academic Publishing
Ähnlichkeitssuche: Fact®Finder von OMIKRON