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2008 | 1 |
2017 | 1 |
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Page 1
Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review.
Genes (Basel). 2022 Dec 16;13(12):2377. doi: 10.3390/genes13122377.
Genes (Basel). 2022.
PMID: 36553645
Free PMC article.
Review.
Hypercalcemia in children: three cases report with unusual clinical presentations.
Garbim BB, D Ávila L, Rigatto SZP, Quadros KRDS, Belangero VMS, Oliveira RB.
Garbim BB, et al. Among authors: rigatto szp.
J Bras Nefrol. 2017 Apr-Jun;39(2):213-216. doi: 10.5935/0101-2800.20170036.
J Bras Nefrol. 2017.
PMID: 29069246
Free article.
English, Portuguese.
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Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.
Coeli FB, Ferraz LF, Lemos-Marini SH, Rigatto SZ, Belangero VM, de-Mello MP.
Coeli FB, et al. Among authors: rigatto sz.
Arq Bras Endocrinol Metabol. 2008 Nov;52(8):1277-81. doi: 10.1590/s0004-27302008000800012.
Arq Bras Endocrinol Metabol. 2008.
PMID: 19169481
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