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2. Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion Syndrome

8. Morquio‐like dysostosis multiplex presenting with neuronopathic features is a distinctGLB1‐related phenotype

11. Genetic investigation of patients with tall stature

19. IFT46 plays an essential role in cilia development

21. Manganese analysis of sorghum hybrid (Sorghum bicolor (L) Moench) on different lamp current using an atomic absorption spectrophotometer

22. An Application of Computerized Asthma-Specific QOL in Korean Asthmatics

24. P-006

25. Associations among genotype, clinical phenotype, and intracellular localization of trafficking proteins in ARC syndrome

26. Ocular manifestations of Noonan syndrome

29. Mucopolysaccharidosis I, II, and VI: brief review and guidelines for treatment

36. Serum leptin level is a regulator of bone mass

37. Williams-Beuren syndrome: cardiovascular abnormalities in 20 patients diagnosed with fluorescence in situ hybridization

39. Cardiac findings in 31 patients with Noonan's syndrome

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