39 results on '"Ulucan, H."'
Search Results
2. Changing mechanisms behind domestic violence against women during the COVID-19 pandemic
3. Conclusions of cooperative and noncooperative interaction between monetary and fiscal policies in small scale open economy
4. Segregational fidelity of chromosomes in human thyroid tumour cells
5. ADD(20)(13) IN A GIRL WITH FACIAL DYSMORPHISM AND MENTAL/MOTOR RETARDATION: N01
6. PARTIAL TRISOMY 6P DUE TO MATERNAL T(6;18) TRANSLOCATION IN A BOY WITH FACIAL DYSMORPHISM AND DEVELOPMENTAL DELAY: N02
7. IDENTIFICATION OF SUBTELOMERIC ALTERATIONS BY MLPA IN PATIENTS WITH CORPUS CALLOSUM DYGENESIS: L01
8. A RARE VARIANT OF MICHELIN TIRE SYNDROME IN A GIRL OF FIRST COUSINS: A88
9. ANALYSIS OF TWO PATIENTS WITH DESBUQUOIS DYSPLASIA: A85
10. A CASE OF HEMIPARESIS, HEMIHYPOPLASIA, AND ATHETOID POSTURE WITH UNILATERAL VISION LOSS - AN EXAMPLE OF A VERY RARE DISORDER: FAMILIAL PORENCEPHALY: A55
11. What Is the Important Point Related to Follow-Up Sonographic Evaluation for the Developmental Dysplasia of the Hip?
12. Novel parkin mutations detected in patients with early-onset Parkinson's disease
13. Transient Neonatal Diabetes Mellitus: A Patient Report
14. Health-led growth hypothesis and health financing systems: an econometric synthesis for OECD countries.
15. A novel mutation in FK506 binding protein-like (FKBPL) causes male infertility.
16. DNA repair gene XPD Asp312Asn and XRCC4 G-1394T polymorphisms and the risk of autism spectrum disorder.
17. Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.
18. Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
19. Whole-exome sequencing revealed two novel mutations in Usher syndrome.
20. Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes.
21. Poikiloderma with neutropenia: genotype-ethnic origin correlation, expanding phenotype and literature review.
22. A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve-Melchior-Clausen syndrome.
23. Familial sick sinus syndrome.
24. A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication.
25. Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndrome.
26. A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia.
27. Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene.
28. Incomplete Currarino triad as an embryological variant. Case report and review of the literature.
29. De novo pericentric inversion of chromosome 5 in a girl with mental retardation and unilateral ear malformation.
30. Acrocallosal syndrome: report of five Turkish patients.
31. Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G.
32. A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.
33. Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?
34. Analysis of DNA damage using the comet assay in infants fed cow's milk.
35. Comparative analysis of two thyroid tumor cell lines by fluorescence in situ hybridization and comparative genomic hybridization.
36. Unilateral split foot, torticollis, congenital heart defect and hydrocephaly: a new syndrome?
37. Preliminary study on DNA damage in non breast-fed infants.
38. Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?
39. Evaluation of DNA damage using the comet assay in children on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever.
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