Digitale Bibliotheek
Sluiten Bladeren door artikelen uit een tijdschrift
     Tijdschrift beschrijving
       Alle jaargangen van het bijbehorende tijdschrift
         Alle afleveringen van het bijbehorende jaargang
                                       Alle artikelen van de bijbehorende aflevering
 
                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Analysis of aromatase (CYP19) gene in Iranian women with endometriosis Saber, Hajar
2013
14 2 p. 165-169
5 p.
artikel
2 Association between the polymorphisms of matrix metalloproteinases 9 and 3 genes and risk of myocardial infarction in Egyptian patients Sewelam, Nadia I
2013
14 2 p. 143-148
6 p.
artikel
3 Basic concepts of medical genetics, pathogenetics, part 3 Salem, Mohammad Saad Zaghloul
2013
14 2 p. 209-212
4 p.
artikel
4 Clinical characteristics and analysis of HFE gene variants (C282Y and H63D) in Jordanian Arab patients with age-related macular degeneration Alkhateeb, Asem
2013
14 2 p. 177-181
5 p.
artikel
5 Computational evaluation of small molecule inhibitors of RGS4 to regulate the dopaminergic control of striatal LTD Gaonkar, Krutika Satish
2013
14 2 p. 135-142
8 p.
artikel
6 Consanguinity and its relevance to clinical genetics Shawky, Rabah M.
2013
14 2 p. 157-164
8 p.
artikel
7 Editorial Board 2013
14 2 p. iii-iv
nvt p.
artikel
8 Efficacy of adhesive taping in controlling genu recurvatum in diplegic children: A pilot study Ghalwash, Asmaa M.
2013
14 2 p. 183-188
6 p.
artikel
9 Evaluation of micronucleus frequency by acridine orange fluorescent staining in bucccal epithelial cells of oral submucosus fibrosis (OSMF) patients Jyoti, Smita
2013
14 2 p. 189-193
5 p.
artikel
10 Gene frequency of sickle cell trait among Muslim populations in a Malarial belt of India, i.e., Manipur Shah, Ahsana
2013
14 2 p. 207-208
2 p.
artikel
11 Helium Neon laser therapy for post mastectomy lymphedema and shoulder mobility Khalaf, Mohamed M.
2013
14 2 p. 195-199
5 p.
artikel
12 Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome Tomoum, Hoda
2013
14 2 p. 201-203
3 p.
artikel
13 Letter to the editor: Controversial report on sickle cell trait in Manipur, India Singh, Maishnam Rustam
2013
14 2 p. 205-206
2 p.
artikel
14 Novel mutation predicted to disrupt SGOL1 protein function Gupta, Rohit
2013
14 2 p. 149-155
7 p.
artikel
15 Single nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service Fareed, Mohd
2013
14 2 p. 123-134
12 p.
artikel
16 Telomerase activity and apoptosis genes as parameters of lymphocyte aging in Down syndrome patients Abdel-Salam, Ekram
2013
14 2 p. 171-176
6 p.
artikel
                             16 gevonden resultaten
 
 Koninklijke Bibliotheek - Nationale Bibliotheek van Nederland