Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A.

scientific article published on February 1992

Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1210/JC.74.2.368
P698PubMed publication ID1346145
P5875ResearchGate publication ID21809855

P2093author name stringGenel M
Kidd KK
Flynn SD
Wu JS
Kidd JR
Pakstis AJ
Lichter JB
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectmultiple endocrine neoplasiaQ1553018
P304page(s)368-373
P577publication date1992-02-01
P1433published inThe Journal of Clinical Endocrinology and MetabolismQ3186902
P1476titlePresymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A.
P478volume74

Reverse relations

cites work (P2860)
Q36741066A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus
Q41202102Application of genetic screening information to the management of medullary thyroid carcinoma and multiple endocrine neoplasia type 2.
Q71831501Clinical use of molecular information in the management of multiple endocrine neoplasia type 2A
Q35275653Early diagnosis of the multiple endocrine neoplasia type 2 syndrome: consensus statement. European Community Concerted Action: Medullary Thyroid Carcinoma
Q64459168Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: Implications for therapy
Q78254404Familial medullary thyroid carcinoma: presymptomatic diagnosis and management in children
Q72692491Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A
Q40422434RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma
Q35194481The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred.

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