I agree that this site is using cookies. You can find further informations here.
X
Natália Duarte Linhares
128  results:
Search for persons X
?
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

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/..
 
?
7

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/..
 
?
8

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/..
 
?
9

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/..
 
?
10

1p13.2 deletion displays clinical features overlapping Noon..:

Natália Duarte Linhares ; Maíra Cristina Menezes Freire ; Raony Guimarães Corrêa do Carmo Lisboa Cardenas...
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572016000300349&lng=en&tlng=en.  ,
Link: https://doi.org/10.1590/..
 
?
11

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...
 
?
12

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..
 
?
13

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...
 
?
14

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..
 
?
15

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..
 
1-15