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机译:
Endocrine Practice, Molecular Laboratory, Bruckenstr.21, 69120 Heidelberg, Germany.;
机译:Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism.
机译:Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis
机译:Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia
机译:NEW RECOMMENDATIONS FOR THE QUALITY AND SAFETY OF TISSUES AND CELLS FOR CLINICAL APPLICATION AND ITS SIGNIFICANCE FOR THE PRACTICE OF TISSUE ESTABLISHMENTS PERFORMING CRYOPRESERVATION
机译:Statistical Methods for Wearable Device Data: Applications in Clinical Studies =可穿戴设备数据的统计分析方法及其在临床研究中的应用
机译:HYpERpaRaTHYROID基因:序列REVEaL解答和问题
机译:Coenzyme Q10 Therapy in Hereditary motor sensory Neuropathy Type VI with Novel mitofusin 2 mutation
机译:关于phanta for Clinical Neutron Dosimetry