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Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).
Orphanet J Rare Dis. 2022 Feb 24;17(1):84. doi: 10.1186/s13023-022-02254-4.
Orphanet J Rare Dis. 2022.
PMID: 35209917
Free PMC article.
Clinical, radiographic, and genetic observations in 2 families with cleidocranial dysplasia.
Mestre VF, Spoladori IC, Osiak LB, Paiva WJM, Ferreira de Lima RL, Silveira BC, Salles MJS.
Mestre VF, et al. Among authors: paiva wjm.
Gen Dent. 2022 Jul-Aug;70(4):59-66.
Gen Dent. 2022.
PMID: 35749249
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Partial monosomy of chromosome 21 and congenital malformations monosomy of chromosome 21 and malformations.
Osiak L, Saraiva JG, Mestre VF, Ferrari LSL, Paiva WJM, de Lima RLLF, Salles MJS.
Osiak L, et al. Among authors: paiva wjm.
Clin Dysmorphol. 2020 Jul;29(3):165-166. doi: 10.1097/MCD.0000000000000310.
Clin Dysmorphol. 2020.
PMID: 32501867
No abstract available.
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