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Freitas, Érika L.
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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..
 
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