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Search Results - Cherulli, Bruno L B
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Pendred syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 gene
by
Lofrano-Porto, Adriana
,
Barra, Gustavo B
,
Nascimento, Paula P
,
Costa, PatrĂcia G G
,
Garcia, Erica C
,
Vaz, Rodrigo F
,
Batista, Ana R T
,
Freitas, Ana C R de
,
Cherulli, Bruno L B
,
Bahmad, Jr, Fayez
,
Figueiredo, Larissa G
,
Neves, Francisco A R
,
Casulari, Luiz Augusto
Published in
Arquivos brasileiros de endocrinologia e metabologia
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Arquivos Brasileiros De Endocrinologia E Metabologia
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Adult
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Amino Acid Sequence
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Brazil
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Case-Control Studies
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Consanguinity
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Endocrinology & Metabolism
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Female
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Goiter
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Goiter - Congenital
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Goiter - Genetics
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Hearing Loss, Sensorineural - Congenital
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Hearing Loss, Sensorineural - Genetics
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Homozygote
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Humans
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Hypothyroidism - Genetics
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Male
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Membrane Transport Proteins - Genetics
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Middle Aged
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Mutation - Genetics
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Pedigree
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Road: Directory Of Open Access Scholarly Resources
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Ezb Free E-Journals
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Scielo Brazil
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