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Krepischi, Ana CV
126
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Search for persons
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Online (126)
Mediatypes
Articles (Online) (115)
Bookchapter (Online) (2)
OpenAccess-fulltext (9)
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Sorted by: Year
?
1
Functional assessment of donated human embryos for the gene..:
Ceschin, Ianaê I
;
Ceschin, Alvaro P
;
Joya, Maria S
...
Reproductive BioMedicine Online. 46 (2023) 3 - p. 491-501 , 2023
Link:
https://doi.org/10.1016/..
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2
Pathogenic copy number variants in patients with congenital..:
Correa, Fernanda A.
;
Jorge, Alexander AL
;
Nakaguma, Marilena
...
Clinical Endocrinology. 88 (2018) 3 - p. 425-431 , 2018
Link:
https://doi.org/10.1111/..
?
3
KIF11 microdeletion is associated with microcephaly, chorio..:
Malvezzi, João VM
;
H Magalhaes, Ingrid
;
S Costa, Silvia
...
Human Genome Variation. 5 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
4
Co-expression network of neural-differentiation genes shows..:
Maschietto, Mariana
;
Tahira, Ana C
;
Puga, Renato
...
BMC Medical Genomics. 8 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
5
The profile and contribution of rare germline copy number v..:
Silva, Amanda G
;
Krepischi, Ana CV
;
Pearson, Peter L
...
Orphanet Journal of Rare Diseases. 9 (2014) 1 - p. 63 , 2014
Link:
https://doi.org/10.1186/..
?
6
Mutational spectrum of WTX, WT1, CTNNB1, APC and PLCG2 gene..:
Barros, Bruna D
;
Torrezan, Giovana T
;
Ferreira, Elisa N
...
BMC Proceedings. 6 (2012) S6 - p. , 2012
Link:
https://doi.org/10.1186/..
?
7
Number of rare germline CNVs and TP53 mutation types:
Silva, Amanda G
;
Achatz, Maria Isabel Waddington
;
Krepischi, Ana CV
..
Orphanet Journal of Rare Diseases. 7 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
?
8
Germline DNA copy number variation in familial and early-on..:
Krepischi, Ana CV
;
Achatz, Maria Isabel W
;
Santos, Erika MM
...
Breast Cancer Research. 14 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
?
9
Breakpoint characterization of a novel large intragenic del..:
Torrezan, Giovana T
;
da Silva, Felipe CC
;
Krepischi, Ana CV
...
BMC Medical Genetics. 12 (2011) 1 - p. , 2011
Link:
https://doi.org/10.1186/..
?
10
Methylome profiling of healthy and central precocious puber..:
Bessa, Danielle, S
;
Maschietto, Mariana
;
Aylwin, Carlos, Francisco
...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s13148-018-0581-1. , 2018
Link:
https://hal.sorbonne-uni..
?
11
Differential DNA Methylation of MicroRNA Genes in Temporal ..:
Villela, Darine
;
Ramalho, Rodrigo F
;
Silva, Aderbal RT
...
qt0m86n4q9. , 2016
Link:
https://escholarship.org..
?
12
The profile and contribution of rare germline copy number v..:
Silva, Amanda G
;
Krepischi, Ana CV
;
Pearson, Peter L
...
http://www.ojrd.com/content/9/1/63. , 2014
Link:
http://www.ojrd.com/cont..
?
13
Number of rare germline CNVs and TP53 mutation types:
Silva Amanda G
;
Achatz Isabel Maria W
;
Krepischi Ana CV
..
http://www.ojrd.com/content/7/1/101. , 2012
Link:
https://doi.org/10.1186/..
?
14
Germline DNA copy number variation in familial and early-on..:
Krepischi, Ana CV
;
Achatz, Maria Isabel W
;
Santos, Erika MM
...
http://breast-cancer-research.com/content/14/1/R24. , 2012
Link:
http://breast-cancer-res..
?
15
Mutational spectrum of WTX, WT1, CTNNB1, APC and PLCG2 gene..:
Barros, Bruna D
;
Torrezan, Giovana T
;
Ferreira, Elisa N
...
http://www.biomedcentral.com/1753-6561/6/S6/P52. , 2012
Link:
http://www.biomedcentral..
1-15