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Linhares, Natália Duarte
127
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Online (127)
Mediatypes
Articles (Online) (108)
Bookchapter (Online) (3)
OpenAccess-fulltext (16)
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?
1
Mild Phenotype of Arthrogryposis, Renal Dysfunction, and Ch..:
Linhares, Natália Duarte
;
Fagundes, Eleonora Druve Tavares
;
Ferreira, Alexandre Rodrigues
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
2
Editorial: Improving medical diagnosis in rare diseases:
Linhares, Natália Duarte
;
Gorman, Kathleen M
;
Brusco, Alfredo
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
3
De novo loss-of-function variants in X-linked MED12 are ass..:
Li, Dong
;
Strong, Alanna
;
Shen, Kaitlyn M.
...
Genetics in Medicine. 23 (2021) 4 - p. 637-644 , 2021
Link:
https://doi.org/10.1038/..
?
4
Nephrotic syndrome and adrenal insufficiency caused by a va..:
Linhares, Natália Duarte
;
Arantes, Rodrigo Rezende
;
Araujo, Stanley Almeida
.
Clinical Kidney Journal. 11 (2017) 4 - p. 462-467 , 2017
Link:
https://doi.org/10.1093/..
?
5
Mendel,MD: a user-friendly online program for clinical exom..:
Cardenas, Raony Guimarães Corrêa Do Carmo Lis
;
Duarte Linhares, Natália
;
Junho Pena, Sérgio D
BMC Bioinformatics. 16 (2015) S8 - p. , 2015
Link:
https://doi.org/10.1186/..
?
6
Editorial: Improving medical diagnosis in rare diseases:
Linhares, Natália Duarte
;
Gorman, Kathleen M
;
Brusco, Alfredo
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486316/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
7
Editorial: Improving medical diagnosis in rare diseases:
Linhares, Natália Duarte
;
Gorman, Kathleen M
;
Brusco, Alfredo
info:eu-repo/semantics/altIdentifier/pmid/36147485. , 2022
Link:
https://hdl.handle.net/2..
?
8
Nephrotic syndrome and adrenal insufficiency caused by a va..:
Linhares, Natália Duarte
;
Arantes, Rodrigo Rezende
;
Araujo, Stanley Almeida
.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070023/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
9
1p13.2 deletion displays clinical features overlapping Noon..:
Linhares, Natalia Duarte
;
Menezes Freire, Maira Cristina
;
do Carmo Lisboa Cardenas, Raony Guimaraes Correa
...
Genetics and Molecular Biology, 1415-4757, 2016, 39:3, s. 349-357. , 2016
Link:
http://urn.kb.se/resolve..
?
10
1p13.2 deletion displays clinical features overlapping Noon..:
Linhares, Natália Duarte
;
Freire, Maíra Cristina Menezes
;
Cardenas, Raony Guimarães Corrêa do Carmo Lis
...
https://eprints.soton.ac.uk/402671/1/1415-4757-gmb-1678-4685-GMB-2016-0049.pdf. , 2016
Link:
https://eprints.soton.ac..
?
11
Mild Phenotype of Arthrogryposis, Renal Dysfunction, and Ch..:
Natália Duarte Linhares
;
Eleonora Druve Tavares Fagundes
;
Alexandre Rodrigues Ferreira
...
https://www.frontiersin.org/articles/10.3389/fgene.2022.796759/full. , 2022
Link:
https://doi.org/10.3389/..
?
12
Table1_Mild Phenotype of Arthrogryposis, Renal Dysfunction,..:
Natália Duarte Linhares
;
Eleonora Druve Tavares Fagundes
;
Alexandre Rodrigues Ferreira
...
doi:10.3389/fgene.2022.796759.s001. , 2022
Link:
https://doi.org/10.3389/..
?
13
Editorial: Improving medical diagnosis in rare diseases:
Natália Duarte Linhares
;
Kathleen M Gorman
;
Alfredo Brusco
https://www.frontiersin.org/articles/10.3389/fgene.2022.974129/full. , 2022
Link:
https://doi.org/10.3389/..
?
14
Mendel,MD: a user-friendly online program for clinical exom..:
Guimarães Corrêa Do Carmo Lisboa Cardenas, Raony
;
Duarte Linhares, Natália
;
Junho Pena, Sérgio D
http://www.biomedcentral.com/1471-2105/16/S8/A2. , 2015
Link:
http://www.biomedcentral..
?
15
Diagnóstico citogenético de pacientes com retardo mental id..:
Natália Duarte Linhares
;
Marta Svartman
;
Eugênia Ribeiro Valadares
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1676-24442012000100007. , 2012
Link:
https://doi.org/10.1590/..
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