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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.
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.
de Wallau MB, Xavier AC, Moreno CA, Kim CA, Mendes EL, Ribeiro EM, Oliveira A, Félix TM, Fett-Conte AC, Bonadia LC, Correia-Costa GR, Monlleó IL, Gil-da-Silva-Lopes VL, Vieira TP.
de Wallau MB, et al. Among authors: correia costa gr.
Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518.
Genes (Basel). 2024.
PMID: 38674452
Free PMC article.
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Biallelic frameshift variant in the TBC1D2B gene in two siblings with progressive gingival overgrowth, fibrous dysplasia of face, and mental deterioration.
Correia-Costa GR, de Leeuw N, Pfundt R, Sgardioli IC, Dos Santos AP, de Lima Santos M, Gil-da-Silva-Lopes VL, Vieira TP.
Correia-Costa GR, et al.
Clin Genet. 2022 Dec;102(6):537-542. doi: 10.1111/cge.14215. Epub 2022 Sep 7.
Clin Genet. 2022.
PMID: 36029130
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Increased runs of homozygosity in the autosomal genome of Brazilian individuals with neurodevelopmental delay/intellectual disability and/or multiple congenital anomalies investigated by chromosomal microarray analysis.
Correia-Costa GR, Sgardioli IC, Santos APD, Araujo TK, Secolin R, Lopes-Cendes I, Gil-da-Silva-Lopes VL, Vieira TP.
Correia-Costa GR, et al.
Genet Mol Biol. 2022 Feb 28;45(1):e20200480. doi: 10.1590/1678-4685-GMB-2020-0480. eCollection 2022.
Genet Mol Biol. 2022.
PMID: 35238326
Free PMC article.
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