References
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Brauer V F, Scholz G H, Neumann S, Lohmann T, Paschke R, Koch C A.
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Ito S, Iwashita T, Asai N, Murakami H, Iwata Y, Sobue G, Takahashi M.
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Iwashita T, Kato M, Murakami H, Asai N, Ishiguro Y, Ito S, Iwata Y, Kawai K, Asai M, Kurokawa K, Kajita H, Takahashi M.
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11
Kitamura Y, Scavarda N, Wells Jr S A, Jackson C E, Goodfellow P J.
Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2B.
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12
Koch C A, Huang S C, Vortmeyer A O, Zhuang Z, Chrousos G P, Pacak K.
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Menko F H, van der Luijt R B, de Valk I A, Toorians A W, Sepers J M, van Diest P J, Lips C J.
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918.
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14
Miyauchi A, Futami H, Hai N, Yokozawa T, Kuma K, Aoki N, Kosugi S, Sugano K, Yamaguchi K.
Two germline missense mutations at codons 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation.
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15
Nunes A B, Ezabella M C, Pereira A C, Krieger J E, Toledo S P.
A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma.
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Poturnajova M, Altanerova V, Kostalova L, Breza J, Altaner C.
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17
Robledo M, Gil L, Pollan M, Cebrian A, Ruiz S, Azanedo M, Benitez J, Menarguez J, Rojas J M.
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Tessitore A, Sinisi A A, Pasquali D, Cardone M, Vitale D, Bellastella A, Colantuoni V.
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S. Dvorakova
Institute of Endocrinology
Department of Molecular Endokrinology
Narodni 8
Prague 1
Czech Republic
Phone: + 420224905301
Fax: + 42 02 24 90 53 25
Email: sarka@obloha.cz