E-LIB Suche - Ergebnisse für: Miriam Coelho Molck

1

Frequency and Genetic Profile of Compound Heterozygous Frie..:

Peluzzo, Thiago Mazzo ; Bonadia, Luciana Cardoso ; Donatti, Amanda...
The Cerebellum. 18 (2019) 6 - p. 1143-1146 , 2019

2

Copy number variation in the susceptibility to systemic lup..:

Barbosa, Fernanda Bueno ; Simioni, Milena ; Wiezel, Cláudia Emília Vieira...
PLOS ONE. 13 (2018) 11 - p. e0206683 , 2018

Link: https://doi.org/10.1371/..

3

Genomic imbalances in syndromic congenital heart disease:

Molck, Miriam Coelho ; Simioni, Milena ; Paiva Vieira, Társis...
Jornal de Pediatria. 93 (2017) 5 - p. 497-507 , 2017

Link: https://doi.org/10.1016/..

4

Genomic imbalances in syndromic congenital heart disease:

Coelho Molck, Miriam ; Simioni, Milena ; Vieira, Társis Paiva...
Jornal de Pediatria (Versão em Português). 93 (2017) 5 - p. 497-507 , 2017

Link: https://doi.org/10.1016/..

5

Distal 22q11.2 microduplication combined with typical 22q11..:

Molck, Miriam Coelho ; Vieira, Társis Paiva ; Simioni, Milena...
American Journal of Medical Genetics Part A. 167 (2014) 1 - p. 215-220 , 2014

Link: https://doi.org/10.1002/..

6

Chromosomal imbalances exclusively detected in invasive fro..:

Ambrosio, Eliane Papa ; Silveira, Cássia Gisele Terrassani ; Drigo, Sandra Aparecida...
Tumor Biology. 34 (2013) 5 - p. 3015-3026 , 2013

Link: https://doi.org/10.1007/..

7

Atypical copy number abnormalities in 22q11.2 region: Repor..:

Molck, Miriam Coelho ; Vieira, Társis Paiva ; Sgardioli, Ilária Cristina...
European Journal of Medical Genetics. 56 (2013) 9 - p. 515-520 , 2013

Link: https://doi.org/10.1016/..

8

Copy number variation in the susceptibility to systemic lup..:

Fernanda Bueno Barbosa ; Milena Simioni ; Cláudia Emília Vieira Wiezel...
https://doi.org/10.1371/journal.pone.0206683. , 2018

Link: https://doi.org/10.1371/..

9

Genomic imbalances in syndromic congenital heart disease:

Miriam Coelho Molck ; Milena Simioni ; Társis Paiva Vieira...
http://www.sciencedirect.com/science/article/pii/S0021755717302188. , 2017

Link: https://doi.org/10.1016/..

10

Genomic imbalances in syndromic congenital heart disease:

Miriam Coelho Molck ; Milena Simioni ; Társis Paiva Vieira...
http://www.sciencedirect.com/science/article/pii/S2255553617300332. , 2017

Link: https://doi.org/10.1016/..

11

Genomic imbalances in syndromic congenital heart disease:

Miriam Coelho Molck ; Milena Simioni ; Társis Paiva Vieira...
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572017000500497&lng=en&tlng=en. ,

Link: https://doi.org/10.1016/..

12

Loss of heterozygosity (LOH) Analysis in individuals with d..:

Sgardioli, Ilária Cristina ; Molck, Miriam Coelho ; Copelli, Matheus de Mello..
https://ojs.uel.br/revistas/uel/index.php/seminabio/article/view/29486/22540. , 2018

Link: https://ojs.uel.br/revis..

13

Genomic imbalances in syndromic congenital heart disease:

Molck, Miriam Coelho ; Simioni, Milena ; Vieira, Társis Paiva...
10.1016/j.jped.2016.11.007. , 2017

Link: http://www.scielo.br/sci..

14

Ancestry Informative Marker Panel to Estimate Population St..:

Barbosa, Fernanda B. ; Cagnin, Natalia F. ; Simioni, Milena...
Annals of Human Genetics. 81 (2017) 6 - p. 225-233 , 2017

Link: https://doi.org/10.1111/..

15

Genotype‐phenotype correlation of 16p13.3 terminal duplicat..:

Fontes, Marshall I. B. ; Santos, Ana P. ; Molck, Miriam C....
American Journal of Medical Genetics Part A. 170 (2015) 3 - p. 766-772 , 2015

Link: https://doi.org/10.1002/..