RLIP76 Gene Variants are not Associated with Drug Response in Turkish Epilepsy Patients

por Manguoğlu, E, Akdeniz, S, Dündar, NO, Duman, Ö, Aktekin, B, Haspolat, Ş, Bilge, U, Özel, D, Lüleci, G
Publicado 2011

Aplasia Ras Homologous Member I Gene and Development of Glial Tumors

por Yakut, S, Tuncer, MR, Berker, M, Goksu, E, Gurer, I, Ozes, ON, Luleci, G, Karauzum, SB
Publicado 2011

Molecular Genetic Characterization of β-Thalassemia and Sickle Cell Syndrome in the Albanian Population

por Babameto-Laku, A, Mitre, A, Berisha, S, Mokini, V, Roko, D
Publicado 2011

Interleukin-18 Promoter Gene Polymorphisms are not Associated with Myocardial Infarction in Type 2 Diabetes in Slovenia

por Kariž, S, Petrovič, D
Publicado 2011

Partial Trisomy 9p(p22→pter) from a Maternal Translocation 4q35 and 9p22

por Mahjoubi, F, Nasiri, F, Torabi, R
Publicado 2011

Individual Phenotype Trait Variability as Genetic Markers of Gender Susceptibility to Spina Bifida

por Nikolic, DP, Cvjeticanin, S, Petronic, I, Brdar, R, Cirovic, D, Bizic, M, Milincic, Z, Karan, R
Publicado 2011

Stem Cells: A Personal Perspective

por Wong, SC
Publicado 2011

Hypergonadotropic Hypogonadism, Progressive Early-Onset Spinocerebellar Ataxia, and Late-Onset Sensorineural Hearing Loss: Case Report and Literature Review

por Sarikaya, E, Ensert, CG, Gulerman, HC
Publicado 2011

IL-18 Gene Promoter Region 607C/A Polymorphism in HIV-1 Infected North Indian Population

por Sobti, RC, Sharma, VL, Abitew, AM, Berhane, N, Mahdi, SA, Askari, M, Kuttiat, VS, Wanchu, A
Publicado 2011

Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements

por Liehr, T, Kosayakova, N, Schröder, J, Ziegler, M, Kreskowski, K, Pohle, B, Bhatt, S, Theuss, L, Wilhelm, K, Weise, A, Mrasek, K
Publicado 2011

Alterations of Copy Number of Methylation Pattern in Mismatch Repair Genes by Methylation Specific-Multiplex Ligation-Dependent Probe Amplification in Cases of Colon Cancer

por Onrat, ST, Çeken, I, Ellidokuz, E, Kupelioğlu, A
Publicado 2011

Metadata Management and Semantics in Microarray Repositories

por Kocabaş, F, Can, T, Baykal, N
Publicado 2011

Molecular Analysis of Ring Y Chromosome in a 10-Year-Old Boy with Mixed Gonadal Dysgenesis and Growth Hormone Deficiency

por Milenkovic, T, Guc-Scekic, M, Zdravkovic, D, Topic, V, Liehr, T, Joksic, G, Radivojevic, D, Lakic, N
Publicado 2011

Role of the APOB Gene Polymorphism (c.12669G>A, p. Gln4154Lys) in Coronary Artery Disease in the Indian Punjabi Population

por Sharma, R, Mahajan, M, Singh, B, Singh, G, Singh, P
Publicado 2011

Diagnosis of Fanconi’s Anemia by Diepoxybutane Analysis in Children from Serbia

por Cirkovic, S, Guc-Scekic, M, Vujic, D, Ilic, N, Micic, D, Skoric, D, Jovanovic, A
Publicado 2011

Amplification of c-MYC and MLL Genes as a Marker of Clonal Cell Progression in Patients with Myeloid Malignancy and Trisomy of Chromosomes 8 or 11

por Angelova, S, Jordanova, M, Spassov, B, Shivarov, V, Simeonova, M, Christov, I, Angelova, P, Alexandrova, K, Stoimenov, A, Nikolova, V, Dimova, I, Ganeva, P, Tzvetkov, N, Hadjiev, E, Toshkov, S
Publicado 2011

Stem Cells for Periodontal Regeneration

por Pejcic, A, Kojovic, D, Mirkovic, D, Minic, I
Publicado 201

Human Ring Chromosomes – New Insights for their Clinical Significance

por Guilherme, RS, Klein, E, Hamid, AB, Bhatt, S, Volleth, M, Polityko, A, Kulpanovich, A, Dufke, A, Albrecht, B, Morlot, S, Brecevic, L, Petersen, MB, Manolakos, E, Kosyakova, N, Liehr, T
Publicado 201

Association Between Loss of Dp140 and Cognitive Impairment in Duchenne and Becker Dystrophies

por Chamova, T, Guergueltcheva, V, Raycheva, M, Todorov, T, Genova, J, Bichev, S, Bojinova, V, Mitev, V, Tournev, I, Todorova, A
Publicado 201

MTHFR C677T and A1298C Genotypes and Haplotypes in Slovenian Couples with Unexplained Infertility Problems and in Embryonic Tissues from Spontaneous Abortions

por Stangler Herodež, Š, Zagradišnik, B, Erjavec Škerget, A, Zagorac, A, Takač, I, Vlaisavljević, V, Lokar, L, Kokalj Vokač, N
Publicado 201