Genetic defects associated with familial and sporadic hyperparathyroidism.

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作者： Geoffrey N,Hendy ^[1] ; David E C,Cole

作者单位： Departments of Medicine, Physiology and Human Genetics, McGill University, and Calcium Research Laboratory and Hormones and Cancer Research Unit, Royal Victoria Hospital, Montreal, Quebec, Canada. geoffrey.hendy @ mcgill.ca ^[1]

主题词细胞周期蛋白D1(Cyclin D1);周期素依赖激酶抑制剂p27(Cyclin-Dependent Kinase Inhibitor p27);女(雌)性(Female);人类(Humans);高钙血症(Hypercalcemia);甲状旁腺功能亢进, 原发性(Hyperparathyroidism, Primary);婴儿, 新生(Infant, Newborn);婴儿, 新生, 疾病(Infant, Newborn, Diseases);颌肿瘤(Jaw Neoplasms);杂合子丢失(Loss of Heterozygosity);男(雄)性(Male);多发性内分泌瘤病1型(Multiple Endocrine Neoplasia Type 1);多发性内分泌瘤病2a型(Multiple Endocrine Neoplasia Type 2a);甲状旁腺肿瘤(Parathyroid Neoplasms);原癌基因蛋白质类(Proto-Oncogene Proteins);原癌基因蛋白质c-ret(Proto-Oncogene Proteins c-ret);受体, 钙敏感(Receptors, Calcium-Sensing);肿瘤抑制蛋白质类(Tumor Suppressor Proteins)

DOI 10.1159/000345675

PMID 23652676

发布时间 2013-05-08

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Frontiers of hormone research

2013年41卷

149-65页

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Genetic defects associated with familial and sporadic hyperparathyroidism.

Frontiers of hormone research

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Frontiers of hormone research

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Genetic defects associated with familial and sporadic hyperparathyroidism.

Frontiers of hormone research

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Frontiers of hormone research

相关期刊

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