Showing results (31-40 of 127) with videos related to

Sort By:
Pageof 13
European Urology|July 21, 2001
Calcitonin receptor gene polymorphism: a possible genetic marker for patients with calcium oxalate stonesW C Chen, H C Wu, H F Lu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 31, 2001
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patientsF J Tsai, C F Yang, J Y Wu, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Multiple pterygium syndrome: report of one caseD C Liu, F J Tsai, H W Chen, et al.
Molecular Urology|November 2, 2001
No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formationW C Chen, H Y Chen, C D Hsu, et al.
Urological Research|June 9, 2001
Arginine form of p21 gene codon 31 is less prominent in patients with calcium oxalate stoneW C Chen, H F Lu, H Y Chen, et al.
Urological Research|June 9, 2001
Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone diseaseW C Chen, H Y Chen, J Y Wu, et al.
The Journal of Reproductive Medicine|December 29, 2000
Breech deformation complex in neonatesY Y Hsieh, F J Tsai, C C Lin, et al.
Urological Research|February 7, 2002
Lack of evidence for the association of tumor necrosis factor-alpha gene promoter polymorphism with calcium oxalate stone and bladder cancer patientsF J Tsai, H F Lu, L S Yeh, et al.
The Journal of Endocrinology|March 5, 2002
Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutationsJ-Y Wu, S-G Shu, C-F Yang, et al.
BJU International|February 13, 2001
Association of the vitamin D receptor gene start codon Fok I polymorphism with calcium oxalate stone diseaseW C Chen, H Y Chen, H F Lu, et al.
Pageof 13