Linkage analysis has been performed in four pedigrees with multiple endocrine neoplasia type 2A (MEN 2A) or familial medullary thyroid carcinoma (MTC) using pericentromeric chromosome 10 probes. Important information regarding carrier status has been provided in 10 individuals, many of whom would not have been identified by pentagastrin stimulation testing. We have also used pulsed field gel electrophoresis (PFGE) to link the probes H4JRBP and pMCK2 to a 150 kb fragment. Using PFGE, no evidence was found in DNA from lymphocytes of a major DNA rearrangement in two individuals affected with MEN 2A and an individual with MEN 2B compared with normals. Metastatic MTC from one patient has been used to generate a cDNA library which will be used to...
Medullary thyroid carcinoma (MTC) occurs usually in sporadic form, but about a quarter of the cases ...
BACKGROUND: Germline RET gene mutations are causative of multiple endocrine neoplasia (MEN) 2 and m...
Review on Thyroid: Medullary carcinoma, with data on clinics, and the genes involved
We have performed linkage analysis on 32 families with hereditary medullary thyroid cancer (MTC) wil...
A Japanese family of 87 members in five generations with multiple endocrine neoplasia type 2A (MEN 2...
Nine chromosome 10 DNA markers (FNRB, D10S34, D10Z1, MEN203, D10S94, RBP3, D10S15, MBP [48.11], D10S...
Hereditary medullary thyroid carcinoma (MTC) appears in three forms: 1) in association with pheochro...
INTRODUCTION: Multiple Endocrine Neoplasia (MEN) is a rare autosomal dominant disease with frequency...
Linkage analyses were carried out in nine Japanese kindreds with multiple endocrine neoplasia type 2...
Family .screening for medullary thyroid cancer (MTC) is important for detecting members of multiple ...
OBJECTIVE: This study was aimed to demonstrate the clinical benefits of rearranged during transfe...
The Northern Ireland/Australian family with multiple endocrine neoplasia type 2A (MEN 2A) originally...
Introduction Most familial MTC is caused by a germline mutation of the RET proto-oncogene. Rare fa...
We describe the potential benefits and the limitations of the use of highly polymorphic minisatellit...
Twenty-five percent of medullary thyroid cancers (MTC) are familial and inherited as an autosomal do...
Medullary thyroid carcinoma (MTC) occurs usually in sporadic form, but about a quarter of the cases ...
BACKGROUND: Germline RET gene mutations are causative of multiple endocrine neoplasia (MEN) 2 and m...
Review on Thyroid: Medullary carcinoma, with data on clinics, and the genes involved
We have performed linkage analysis on 32 families with hereditary medullary thyroid cancer (MTC) wil...
A Japanese family of 87 members in five generations with multiple endocrine neoplasia type 2A (MEN 2...
Nine chromosome 10 DNA markers (FNRB, D10S34, D10Z1, MEN203, D10S94, RBP3, D10S15, MBP [48.11], D10S...
Hereditary medullary thyroid carcinoma (MTC) appears in three forms: 1) in association with pheochro...
INTRODUCTION: Multiple Endocrine Neoplasia (MEN) is a rare autosomal dominant disease with frequency...
Linkage analyses were carried out in nine Japanese kindreds with multiple endocrine neoplasia type 2...
Family .screening for medullary thyroid cancer (MTC) is important for detecting members of multiple ...
OBJECTIVE: This study was aimed to demonstrate the clinical benefits of rearranged during transfe...
The Northern Ireland/Australian family with multiple endocrine neoplasia type 2A (MEN 2A) originally...
Introduction Most familial MTC is caused by a germline mutation of the RET proto-oncogene. Rare fa...
We describe the potential benefits and the limitations of the use of highly polymorphic minisatellit...
Twenty-five percent of medullary thyroid cancers (MTC) are familial and inherited as an autosomal do...
Medullary thyroid carcinoma (MTC) occurs usually in sporadic form, but about a quarter of the cases ...
BACKGROUND: Germline RET gene mutations are causative of multiple endocrine neoplasia (MEN) 2 and m...
Review on Thyroid: Medullary carcinoma, with data on clinics, and the genes involved