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Freitas, Érika L
1152
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Online (1152)
Mediatypes
E-Books (1)
Articles (Online) (332)
Bookchapter (Online) (12)
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1
Detection of germline variants in Brazilian breast cancer p..:
Guindalini, Rodrigo Santa Cruz
;
Viana, Danilo Vilela
;
Kitajima, João Paulo Fumio Whitaker
...
Scientific Reports. 12 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
2
Genomic monitoring unveil the early detection of the SARS‐C..:
Slavov, Svetoslav N.
;
Patané, José S. L.
;
Bezerra, Rafael dos Santos
...
Journal of Medical Virology. 93 (2021) 12 - p. 6782-6787 , 2021
Link:
https://doi.org/10.1002/..
?
3
Biallelic loss of function variants in ATP1A2 cause hydrops..:
Monteiro, Fabiola P.
;
Curry, Cynthia J.
;
Hevner, Robert
...
European Journal of Medical Genetics. 63 (2020) 1 - p. 103624 , 2020
Link:
https://doi.org/10.1016/..
?
4
Heterozygous loss of function of NR4A2 is associated with i..:
Ramos, Luiza L. P.
;
Monteiro, Fabiola P.
;
Sampaio, Leticia P. B.
...
Clinical Case Reports. 7 (2019) 8 - p. 1582-1584 , 2019
Link:
https://doi.org/10.1002/..
?
5
Zinc Status Biomarkers and Cardiometabolic Risk Factors in ..:
Freitas, Erika
;
Cunha, Aline
;
Aquino, Sephora
...
Nutrients. 9 (2017) 2 - p. 175 , 2017
Link:
https://doi.org/10.3390/..
?
6
A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplicati..:
Uehara, Daniela T
;
Freitas, Érika L
;
Alves, Leandro U
...
Human Genome Variation. 2 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1038/..
?
7
Deletion of the entire POU4F3 gene in a familial case of au..:
Freitas, Érika L.
;
Oiticica, Jeanne
;
Silva, Amanda G.
...
European Journal of Medical Genetics. 57 (2014) 4 - p. 125-128 , 2014
Link:
https://doi.org/10.1016/..
?
8
TBX6, LHX1 and copy number variations in the complex geneti..:
Sandbacka, Maria
;
Laivuori, Hannele
;
Freitas, Érika
...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013
Link:
https://doi.org/10.1186/..
?
9
Non‐overlapping 22q11.2 microdeletions in patients with ocu..:
dos Santos, Pollyanna Almeida Costa
;
de Oliveira, Silviene Fabiana
;
Freitas, Erika L.
...
American Journal of Medical Genetics Part A. 164 (2013) 2 - p. 551-553 , 2013
Link:
https://doi.org/10.1002/..
?
10
A microduplication of 5p15.33 reveals CLPTM1L as a candidat..:
Izzo, Giselle
;
Freitas, Érika L.
;
Krepischi, Ana Cristina V.
...
European Journal of Medical Genetics. 56 (2013) 4 - p. 222-225 , 2013
Link:
https://doi.org/10.1016/..
?
11
A familial case with interstitial 2q36 deletion: Variable p..:
Freitas, Érika L.
;
Gribble, Susan M.
;
Simioni, Milena
...
European Journal of Medical Genetics. 55 (2012) 11 - p. 660-665 , 2012
Link:
https://doi.org/10.1016/..
?
12
Maternally inherited partial monosomy 9p (pter → p24.1) and..:
Freitas, Érika L.
;
Gribble, Susan M.
;
Simioni, Milena
...
American Journal of Medical Genetics Part A. 155 (2011) 11 - p. 2754-2761 , 2011
Link:
https://doi.org/10.1002/..
?
13
Preliminary molecular studies on blepharocheilodontic syndr..:
Freitas, Érika L.
;
Martinhago, Ciro D.
;
Ramos, Ester S.
..
American Journal of Medical Genetics Part A. 143A (2007) 22 - p. 2757-2759 , 2007
Link:
https://doi.org/10.1002/..
?
14
Saethre-Chotzen Syndrome Caused By Q289P Mutation In FGFR2 ..:
Freitas, Erika
;
Nascimento, Sandra
;
Mello, Maricilda
.
The Cleft Palate-Craniofacial Journal. , 2005
Link:
https://doi.org/10.1597/..
?
15
O assessoramento do pedagogo da equipe especializada de apo..:
Macêdo, Lourdes Christina dos Santos de
;
Freitas, Erika Rodrigues de
;
Dantas, Otília Maria Alves da Nóbrega Alberto
CONTRIBUCIONES A LAS CIENCIAS SOCIALES. 17 (2024) 7 - p. e8576 , 2024
Link:
https://doi.org/10.55905..
1-15