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Screening children at risk of developing inherited endocrine neoplasia syndromes
Author(s) -
LB Johnston,
Chew Sl,
Peter J Trainer,
Rodney H. Reznek,
A Grossman,
Besser Gm,
JP Monson,
Savage Mo
Publication year - 2000
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1046/j.1365-2265.2000.00956.x
Subject(s) - penetrance , men1 , medicine , multiple endocrine neoplasia , von hippel–lindau disease , genetic testing , pheochromocytoma , disease , genetic counseling , endocrine system , multiple endocrine neoplasia type 2 , pediatrics , bioinformatics , mutation , pathology , germline mutation , genetics , biology , gene , hormone , phenotype