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Hyperparathyroid genes: sequences reveal answers and questions.

Hyperparathyroid genes: sequences reveal answers and questions.

http://www.wikidata.org/entity/Q34628063

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GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.Pituitary tumors in patients with MEN1 syndrome.Successful treatment of osteitis fibrosa cystica from primary hyperparathyroidism Diagnostic, therapeutic and healthcare management protocols in parathyroid surgery: II Consensus Conference of the Italian Association of Endocrine Surgery Units (U.E.C. CLUB).Rare diseases in clinical endocrinology: a taxonomic classification system.A new look at vitamin D metabolism and "idiopathic" hypercalcemia.Heritable forms of primary hyperparathyroidism: a current perspective.Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism.

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Hyperparathyroid genes: sequences reveal answers and questions.

http://www.wikidata.org/entity/Q34628063

description

2011 nî lūn-bûn

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2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հուլիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Hyperparathyroid genes: sequences reveal answers and questions.

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Endocrine Practice

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Hyperparathyroid genes: sequences reveal answers and questions.

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Stephen J Marx

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P2860

Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia

Activation of a novel human transforming gene, ret, by DNA rearrangement

DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors

Positional cloning of the gene for multiple endocrine neoplasia-type 1

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18-27

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scholarly article

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10.4158/EP11067.RA

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17 Suppl 3

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2011-07-01T00:00:00Z

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21454225

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3484688

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