http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000319529000041&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Medicine, General & InternalSCI(E)PubMed中国科技核心期刊(ISTIC)中国科学引文数据库(CSCD)0LETTER81599-160012
Hereditary medullary thyroid carcinoma (MTC) appears in three forms: 1) in association with pheochro...
Background. Germline missense point mutations of the ret proto-oncogene have been shown as causative...
Context: Over the last decade, our knowledge of the multiple endocrine neoplasia (MEN) type 2 syndro...
BACKGROUND: Germline RET gene mutations are causative of multiple endocrine neoplasia (MEN) 2 and m...
Twenty-five percent of medullary thyroid cancers (MTC) are familial and inherited as an autosomal do...
MEN-2A is characterized by medullary thyroid carcinoma (MTC) with pheochromocytoma and sometimes par...
Objective. To identify by means of genetic analyses individuals who are at risk of developing medull...
Department of Surgery, University Hospital of Maastricht, The Netherlands.BACKGROUND: Patients with ...
Medullary thyroid carcinoma (MTC) occurs usually in sporadic form, but about a quarter of the cases ...
OBJECTIVE: This study was aimed to demonstrate the clinical benefits of rearranged during transfe...
Background: Missense germ-line mutations in the RET protooncogene are associated with multiple endoc...
A Japanese family of 87 members in five generations with multiple endocrine neoplasia type 2A (MEN 2...
Whole exome sequencing provides a labor-saving and direct means of genetic diagnosis of hereditary d...
We have performed linkage analysis on 32 families with hereditary medullary thyroid cancer (MTC) wil...
Medullary thyroid cancer (MTC) is a rare thyroid tumor whose prevalence is 3-5% among all thyroid tu...
Hereditary medullary thyroid carcinoma (MTC) appears in three forms: 1) in association with pheochro...
Background. Germline missense point mutations of the ret proto-oncogene have been shown as causative...
Context: Over the last decade, our knowledge of the multiple endocrine neoplasia (MEN) type 2 syndro...
BACKGROUND: Germline RET gene mutations are causative of multiple endocrine neoplasia (MEN) 2 and m...
Twenty-five percent of medullary thyroid cancers (MTC) are familial and inherited as an autosomal do...
MEN-2A is characterized by medullary thyroid carcinoma (MTC) with pheochromocytoma and sometimes par...
Objective. To identify by means of genetic analyses individuals who are at risk of developing medull...
Department of Surgery, University Hospital of Maastricht, The Netherlands.BACKGROUND: Patients with ...
Medullary thyroid carcinoma (MTC) occurs usually in sporadic form, but about a quarter of the cases ...
OBJECTIVE: This study was aimed to demonstrate the clinical benefits of rearranged during transfe...
Background: Missense germ-line mutations in the RET protooncogene are associated with multiple endoc...
A Japanese family of 87 members in five generations with multiple endocrine neoplasia type 2A (MEN 2...
Whole exome sequencing provides a labor-saving and direct means of genetic diagnosis of hereditary d...
We have performed linkage analysis on 32 families with hereditary medullary thyroid cancer (MTC) wil...
Medullary thyroid cancer (MTC) is a rare thyroid tumor whose prevalence is 3-5% among all thyroid tu...
Hereditary medullary thyroid carcinoma (MTC) appears in three forms: 1) in association with pheochro...
Background. Germline missense point mutations of the ret proto-oncogene have been shown as causative...
Context: Over the last decade, our knowledge of the multiple endocrine neoplasia (MEN) type 2 syndro...