125 results on '"Luleci G"'
Search Results
2. Aplasia Ras Homologous Member I Gene and Development of Glial Tumors
3. Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)
4. Short report. The AIDIT and IMPACT conference 2006: Outcomes and future directions
5. Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma
6. Frequencies of four genetic polymorphisms in the CYP1A2 gene in Turkish population
7. Adenovirus-mediated IKKβKA expression sensitizes prostate carcinoma cells to TRAIL-induced apoptosis
8. The Effect of MDR1 ( ABCB1) Polymorphism on the Pharmacokinetic of Tacrolimus in Turkish Renal Transplant Recipients
9. DIFFERENTIAL MRNA LEVELS OF METASTASIS RELATED GENES NM23-H1, KAI1 AND MKK4 IN OMENTAL METASTASIS OF EPITHELIAL OVARIAN CANCER: C10
10. EVALUATION OF PTEN AND MCL-1 EXPRESSIONS IN NSCLC EXPRESSING WILD-TYPE OR MUTATED EGFR: C09
11. ABNORMAL SIGNAL PATTERNS INVOLVED IN T(12;21) TEL-AML1 IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA PATIENTS: H39
12. TWO CASES WITH RARE CHROMOSOMAL ABNORMALITY OF CHROMOSOME 12p PRESENTING PALLISTER-KILLIAN SYNDROME PHENOTYPE: A18
13. PARTIAL TRISOMY 3q IN A CHILD WITH SACROCOCCEGEAL TERATOMA AND CORNELIA DE LANGE SYNDROME PHENOTYPE: A12
14. Two rare mutations in Turkey: IVS I.130(G–C) and IVS II.848(C–A)
15. Molecular analysis of fragile X syndrome in Antalya Province
16. Del (18p) syndrome with increased nuchal translucency revealed in prenatal diagnosis
17. PARTIAL TRISOMY 3q IN A CHILD WITH SACROCOCCYGEAL TERATOMA AND CORNELIA DE LANGE SYNDROME PHENOTYPE
18. Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families
19. P06.05: Prenatal management, pregnancy and pediatric outcome in fetuses with septated cystic hygroma
20. A somatic origin of homologous Robertsonian translocations and isochromosomes
21. Final Diagnosis in Children with Subclinical Hypothyroidism and Mutation Analysis of the Thyroid Peroxidase Gene (TPO)
22. Effects of Hormone Replacement Therapy (HRT) and Alendronate on Bone Mineral Density (BMD) in Patients With Col 1 A1 Sp 1 Binding Site Polymorphism a Prospective Randomized Study
23. Adenovirus-mediated IKKβKA expression sensitizes prostate carcinoma cells to TRAIL-induced apoptosis
24. Molecular analysis of fragile X syndrome in Antalya Province
25. Molecular Analysis of Beta-Thalassemia and Sickle Cell Anemia in Antalya
26. Rate Limiting Steps of AAV Transduction and Implications for Human Gene Therapy
27. Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism.
28. Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications
29. Relationship between SP1 polymorphism and osteoporosis in beta-thalassemia major patients.
30. RLIP76 Gene Variants are not Associated with Drug Response in Turkish Epilepsy Patients
31. Frequency of Three Hemochromatosis Gene Mutations in Antalya, Turkey
32. AIDIT and IMPACT: building research collaborations in targeted prostate cancer screening
33. De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome
34. Novel cytogenetic findings revealed by conventional cytogenetic and FISH analyses in leukaemia patients
35. IMPACT and AIDIT: Strengthening Research Ties in Eastern Europe
36. b-Thalassemia major associated with Down syndrome
37. Psychological effects of amniocentesis.
38. Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia.
39. Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation.
40. Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease.
41. Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.
42. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
43. Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.
44. A patient with Down syndrome with a de novo derivative chromosome 21.
45. Aberrations of chromosomes 9 and 22 in acute lymphoblastic leukemia cases detected by ES-fluorescence in situ hybridization.
46. Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).
47. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
48. Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype.
49. Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.
50. De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.
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