Nine chromosome 10 DNA markers (FNRB, D10S34, D10Z1, MEN203, D10S94, RBP3, D10S15, MBP [48.11], D10S22) were typed in two large Canadian pedigrees with multiple endocrine neoplasia type 2A (MEN 2A). These markers and the gene for MEN 2A (MEN2A) are believed to be in one linkage group spanning approximately 15 cM (male). MEN203 and D10S94 were informative and tightly linked to MEN2A with no recombinants observed in 26 meiotic events. D10S15 (MCK2), widely used in DNA genotyping predictions, demonstrated two recombinants in these two families. The use of multiple flanking markers increases both the likelihood of informativeness and the accuracy of risk assessments for predictive testing. We were able to assign a risk estimate for all 10 at-ri...
We have designed PCR primers that permit the rapid non-Isotopic detection of mutations in codon 634 ...
The dominantly inherited cancer syndrome multiple endocrineneoplasia type 2A (MEN 2A) is characteriz...
Background: Missense germ-line mutations in the RET protooncogene are associated with multiple endoc...
We have performed linkage analysis on 32 families with hereditary medullary thyroid cancer (MTC) wil...
Attempts to map the locus of the gene (MEN2A) for the multiple endocrine neoplasia type 2A (MEN-2A) ...
Linkage analyses were carried out in nine Japanese kindreds with multiple endocrine neoplasia type 2...
Linkage analysis has been performed in four pedigrees with multiple endocrine neoplasia type 2A (MEN...
A Japanese family of 87 members in five generations with multiple endocrine neoplasia type 2A (MEN 2...
Multiple endocrine neoplasia type 2B (MEN 2B) is similar to MEN 2A in that both autosomal dominant s...
We describe the potential benefits and the limitations of the use of highly polymorphic minisatellit...
The search for the gene that causes the multiple endocrine neoplasia type 2A (MEN 2A) syndrome is en...
SummaryMultiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by...
AbstractBackgroundMultiple endocrine neoplasia type 2A (MEN2A) is a rare cancer associated-syndrome,...
We have analyzed DNA marker typing data contributed by six independent groups to estimate the pairwi...
INTRODUCTION: Multiple Endocrine Neoplasia (MEN) is a rare autosomal dominant disease with frequency...
We have designed PCR primers that permit the rapid non-Isotopic detection of mutations in codon 634 ...
The dominantly inherited cancer syndrome multiple endocrineneoplasia type 2A (MEN 2A) is characteriz...
Background: Missense germ-line mutations in the RET protooncogene are associated with multiple endoc...
We have performed linkage analysis on 32 families with hereditary medullary thyroid cancer (MTC) wil...
Attempts to map the locus of the gene (MEN2A) for the multiple endocrine neoplasia type 2A (MEN-2A) ...
Linkage analyses were carried out in nine Japanese kindreds with multiple endocrine neoplasia type 2...
Linkage analysis has been performed in four pedigrees with multiple endocrine neoplasia type 2A (MEN...
A Japanese family of 87 members in five generations with multiple endocrine neoplasia type 2A (MEN 2...
Multiple endocrine neoplasia type 2B (MEN 2B) is similar to MEN 2A in that both autosomal dominant s...
We describe the potential benefits and the limitations of the use of highly polymorphic minisatellit...
The search for the gene that causes the multiple endocrine neoplasia type 2A (MEN 2A) syndrome is en...
SummaryMultiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by...
AbstractBackgroundMultiple endocrine neoplasia type 2A (MEN2A) is a rare cancer associated-syndrome,...
We have analyzed DNA marker typing data contributed by six independent groups to estimate the pairwi...
INTRODUCTION: Multiple Endocrine Neoplasia (MEN) is a rare autosomal dominant disease with frequency...
We have designed PCR primers that permit the rapid non-Isotopic detection of mutations in codon 634 ...
The dominantly inherited cancer syndrome multiple endocrineneoplasia type 2A (MEN 2A) is characteriz...
Background: Missense germ-line mutations in the RET protooncogene are associated with multiple endoc...