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
Broschiertes Buch
Assessment of HEXA Gene Mutation induced Tay-Sachs disease of Tabriz Population in year 2016 IRAN
21. Oktober 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of Large deletions in Gene VLGR1 causes Ascher syndrome type IIC in male and female patients in Family TABRIZ
19. Oktober 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Assessment of high frequency 35delG Mutation in GJB2-related deafness syndrome in a population without,Tabriz,city,IRAN
11. Oktober 2016
Scholar's Press
Broschiertes Buch
Genetic Mutations in Spinal Muscular Atrophy
20. September 2016
Scholar's Press
Broschiertes Buch
The presence of HLA-DRB1 alleles in children with juvenile rheumatoid arthritis in Tabriz city of IRAN by 2016
9. September 2016
Scholar's Press
Broschiertes Buch
Human Embryonic Heart Development by the four main Genes
23. August 2016
Scholar's Press
Broschiertes Buch
Msx1 gene mutation in women's reproductive delay
8. Juni 2016
LAP Lambert Academic Publishing
Broschiertes Buch
New genetic mutations in breast cancer in women under 28 years Iran
9. Mai 2016
Scholar's Press
Broschiertes Buch
29. März 2016
LAP Lambert Academic Publishing
Broschiertes Buch
Factor 5 Leiden genetic study of cardiovascular disease in young and middle-aged people of Tabriz in Iran
24. Mai 2016
Scholar's Press
Broschiertes Buch
The study of expression of miRNA-133 and miRNA-431b in Breast Cancer
16. Januar 2018
LAP Lambert Academic Publishing
Broschiertes Buch
Avaliação genética Mutações nos genes RNF213, ACTA2, GUCY1A3 que induzem a doença de Moyamoya
18. August 2025
Edições Nosso Conhecimento
Ähnlichkeitssuche: Fact®Finder von OMIKRON
