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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Cardiological assessment of a cohort of Egyptian patients with osteogenesis imperfecta type III ElAbd, Heba Salah A.
2016
17 2 p. 197-200
4 p.
artikel
2 Corrigendum to “A novel nonsense mutation in the cathepsin C gene in an Egyptian patient presenting with Papillon–Lefèvre syndrome” [Egypt. J. Med. Hum. Genet. 16 (4) (2015) 387–392] Soliman, Hala
2016
17 2 p. 239-
1 p.
artikel
3 Cytokine gene polymorphisms and their association with cervical cancer: A North Indian study Gupta, Maneesh Kumar
2016
17 2 p. 155-163
9 p.
artikel
4 Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML Akin, Dilara Fatma
2016
17 2 p. 209-215
7 p.
artikel
5 Editorial Board 2016
17 2 p. iii-
1 p.
artikel
6 Fraser syndrome: Phenotypic variability and unusual findings in four Egyptian families Abdalla, Ebtesam M.
2016
17 2 p. 233-238
6 p.
artikel
7 Griscelli syndrome type 2 – A case report and clinical approach to silver blonde hair Durrani, Sana
2016
17 2 p. 229-232
4 p.
artikel
8 Inducible protective processes in animal systems XIV: Cytogenetic adaptive response induced by EMS or MMS in bone marrow cells of diabetic mouse Khalandar, B.B. Dada
2016
17 2 p. 201-208
8 p.
artikel
9 Inducible protective processes in animal systems XV: Hyperthermia enhances the Ethyl methanesulfonate induced adaptive response in meiotic cells of grasshopper Poecilocerus pictus Venu, R.
2016
17 2 p. 173-184
12 p.
artikel
10 Methionine synthase A2756G and reduced folate carrier1 A80G gene polymorphisms as maternal risk factors for Down syndrome in Egypt Moustafa, Maha
2016
17 2 p. 217-221
5 p.
artikel
11 Molecular characterization of X chromosome fragility in idiopathic mental retardation Hosny Omar, Heba Alla
2016
17 2 p. 165-172
8 p.
artikel
12 Natural killer cells enhance the immune surveillance of cancer Nouroz, Faisal
2016
17 2 p. 149-154
6 p.
artikel
13 Partial association of restriction polymorphism of the ligand binding domain of human androgen receptor in prostate cancer Hessien, Mohamed
2016
17 2 p. 223-228
6 p.
artikel
14 Role of MTHFR A1298C gene polymorphism in the etiology of prostate cancer: A systematic review and updated meta-analysis Yadav, Upendra
2016
17 2 p. 141-148
8 p.
artikel
15 Sirtuin 1 gene rs2273773 C>T single nucleotide polymorphism and protein oxidation markers in asthmatic patients Mahmoud, Aida Abdeen
2016
17 2 p. 191-196
6 p.
artikel
16 The association between (8390G>A) single nucleotide polymorphism in APOE gene with Alzheimer’s and Parkinson disease Mohammadpour Lashkari, Faranak
2016
17 2 p. 185-189
5 p.
artikel
                             16 gevonden resultaten
 
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