Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Vieira, Társis Paiva
84  Ergebnisse:
Personensuche X
?
1

Genome Sequencing in an Individual Presenting with 22q11.2 ..:

de Oliveira-Sobrinho, Ruy Pires ; Appenzeller, Simone ; Holanda, Ianne Pessoa...
Genes.  15 (2024)  4 - p. 513 , 2024
Link: https://doi.org/10.3390/..
 
?
2

Variants in KMT2A in Three Individuals with Previous Suspic..:

Silveira, Henrique Garcia ; Steiner, Carlos Eduardo ; Toccoli, Giovana...
Genes.  15 (2024)  2 - p. 211 , 2024
Link: https://doi.org/10.3390/..
 
?
3

22q11.2 Deletion Syndrome: Influence of Parental Origin on ..:

de Wallau, Melissa Bittencourt ; Xavier, Ana Carolina ; Moreno, Carolina Araújo...
Genes.  15 (2024)  4 - p. 518 , 2024
Link: https://doi.org/10.3390/..
 
?
4

Low‐pass whole genome sequencing as a cost‐effective altern..:

Mazzonetto, Patricia C. ; Villela, Darine ; Krepischi, Ana C. V....
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
?
5

Molecular investigation in individuals with orofacial cleft..:

Atique Tacla, Milena ; de Mello Copelli, Matheus ; Pairet, Eleonore...
European Journal of Human Genetics.  , 2023
Link: https://doi.org/10.1038/..
 
?
6

SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Vari..:

Copelli, Matheus de Mello ; Pairet, Eleonore ; Atique-Tacla, Milena...
Genes.  14 (2023)  4 - p. 882 , 2023
Link: https://doi.org/10.3390/..
 
?
7

Clinical and laboratory differences between chromosomal and..:

Riccetto, Luísa ; Vieira, Tarsis Paiva ; Viguetti-Campos, Nilma Lucia...
Sao Paulo Medical Journal.  141 (2023)  4 - p. , 2023
Link: https://doi.org/10.1590/..
 
?
8

Rare 15q21.1q22.31 Duplication Due to a Familial Chromosoma..:

Nascimento, Carolina Gama ; Prota, Joana Rosa Marques ; Sgardioli, Ilária Cristina...
Genes.  14 (2023)  4 - p. 885 , 2023
Link: https://doi.org/10.3390/..
 
?
9

Dual Molecular Diagnoses of Recessive Disorders in a Child ..:

Correia-Costa, Gabriela Roldão ; dos Santos, Ana Mondadori ; de Leeuw, Nicole...
Genes.  13 (2022)  12 - p. 2377 , 2022
Link: https://doi.org/10.3390/..
 
?
10

Biallelic frameshift variant in the TBC1D2B gene in two sib..:

Correia‐Costa, Gabriela Roldão ; de Leeuw, Nicole ; Pfundt, Rolph...
Clinical Genetics.  102 (2022)  6 - p. 537-542 , 2022
Link: https://doi.org/10.1111/..
 
?
11

Increased runs of homozygosity in the autosomal genome of B..:

Correia-Costa, Gabriela Roldão ; Sgardioli, Ilária Cristina ; Santos, Ana Paula dos...
Genetics and Molecular Biology.  45 (2022)  1 - p. , 2022
Link: https://doi.org/10.1590/..
 
?
12

Further evidence for lack of association of PRDM9 polymorph..:

Carvalho, Pedro Cristovão ; Sgardioli, Ilária Cristina ; Bonadia, Luciana Cardoso...
Meta Gene.  29 (2021)  - p. 100927 , 2021
Link: https://doi.org/10.1016/..
 
?
13

Brazil's Craniofacial Project: Different approaches on orof..:

Gil‐da‐Silva‐Lopes, Vera Lúcia ; Tacla, Milena Atique ; Sgardioli, Ilária Cristina..
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.  184 (2020)  4 - p. 912-927 , 2020
Link: https://doi.org/10.1002/..
 
?
14

Pure 21q22.3 deletion identified in a patient with mild phe..:

Sgardioli, Ilária Cristina ; Copelli, Matheus de Melo ; Lustosa‐Mendes, Elaine..
Congenital Anomalies.  58 (2018)  5 - p. 178-180 , 2018
Link: https://doi.org/10.1111/..
 
?
15

A recognizable phenotype related to 19p13.12 microdeletion:

de Souza, Laiara Cristina ; Sgardioli, Ilária Cristina ; Gil‐da‐Silva‐Lopes, Vera Lúcia.
American Journal of Medical Genetics Part A.  176 (2018)  8 - p. 1753-1759 , 2018
Link: https://doi.org/10.1002/..
 
1-15