Mapping a dominant form of multinodular goiter to chromosome Xp22
about
DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumorsMutational analysis of Peroxiredoxin IV: exclusion of a positional candidate for multinodular goitre.Identification of a KEAP1 germline mutation in a family with multinodular goitreNovel DICER1 mutation as cause of multinodular goiter in children.The pathologist's role in familial nonmedullary thyroid tumors.Molecular pathogenesis of nodular goiter.Etiopathology, clinical features, and treatment of diffuse and multinodular nontoxic goiters.Combined linkage analysis and exome sequencing identifies novel genes for familial goiter.X Chromosome inactivation pattern is not associated with interindividual variations in thyroid volume: a study of euthyroid Danish female twins.
P2860
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P2860
Mapping a dominant form of multinodular goiter to chromosome Xp22
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2000 nî lūn-bûn
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2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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Mapping a dominant form of multinodular goiter to chromosome Xp22
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Mapping a dominant form of multinodular goiter to chromosome Xp22
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Mapping a dominant form of multinodular goiter to chromosome Xp22
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label
Mapping a dominant form of multinodular goiter to chromosome Xp22
@ast
Mapping a dominant form of multinodular goiter to chromosome Xp22
@en
Mapping a dominant form of multinodular goiter to chromosome Xp22
@nl
prefLabel
Mapping a dominant form of multinodular goiter to chromosome Xp22
@ast
Mapping a dominant form of multinodular goiter to chromosome Xp22
@en
Mapping a dominant form of multinodular goiter to chromosome Xp22
@nl
P2093
P2860
P50
P356
P1476
Mapping a dominant form of multinodular goiter to chromosome Xp22
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P2093
P2860
P304
P356
10.1086/303095
P407
P50
P577
2000-09-11T00:00:00Z