Results
|
|
1.
|
|
|
|
2.
|
|
|
|
3.
|
|
|
|
4.
|
|
|
|
5.
|
|
|
|
6.
|
|
|
|
7.
|
|
|
|
8.
|
|
|
|
9.
|
|
|
|
10.
|
|
|
|
11.
|
HLA imputation in an admixed population: An assessment of the 1000 Genomes data as a training set. [electronic resource] by
- Nunes, Kelly
- Zheng, Xiuwen
- Torres, Margareth
- Moraes, Maria Elisa
- Piovezan, Bruno Z
- Pontes, Gerlandia N
- Kimura, Lilian
- Carnavalli, Juliana E P
- Mingroni Netto, Regina C
- Meyer, Diogo
Producer: 20161226
In:
Human immunology vol. 77
Availability: No items available.
|
|
|
12.
|
|
|
|
13.
|
Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in Brazilian populations. [electronic resource] by
- Angeli, Cláudia B
- Kimura, Lilian
- Auricchio, Maria T
- Vicente, João P
- Mattevi, Vanessa S
- Zembrzuski, Verônica M
- Hutz, Mara H
- Pereira, Alexandre C
- Pereira, Tiago V
- Mingroni-Netto, Regina C
Producer: 20110913
In:
Obesity (Silver Spring, Md.) vol. 19
Availability: No items available.
|
|
|
14.
|
|
|
|
15.
|
Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family. [electronic resource] by
- Dantas, Vitor G L
- Freitas, Erika L
- Della-Rosa, Valter A
- Lezirovitz, Karina
- de Moraes, Ana Maria S M
- Ramos, Silvia B
- Oiticica, Jeanne
- Alves, Leandro U
- Pearson, Peter L
- Rosenberg, Carla
- Mingroni-Netto, Regina C
Producer: 20160517
In:
International journal of audiology vol. 54
Availability: No items available.
|
|
|
16.
|
Multivariate meta-analysis of the association of G-protein beta 3 gene (GNB3) haplotypes with cardiovascular phenotypes. [electronic resource] by
- Pereira, Tiago V
- Kimura, Lilian
- Suwazono, Yasushi
- Nakagawa, Hideaki
- Daimon, Makoto
- Oizumi, Toshihide
- Kayama, Takamasa
- Kato, Takeo
- Li, Liao
- Chen, Shufeng
- Gu, Dongfeng
- Renner, Wilfried
- März, Winfried
- Yamada, Yoshiji
- Bagos, Pantelis G
- Mingroni-Netto, Regina C
Producer: 20150105
In:
Molecular biology reports vol. 41
Availability: No items available.
|
|
|
17.
|
Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. [electronic resource] by
- Dantas, Vitor G L
- Raval, Manmeet H
- Ballesteros, Angela
- Cui, Runjia
- Gunther, Laura K
- Yamamoto, Guilherme L
- Alves, Leandro Ucela
- Bueno, André Silva
- Lezirovitz, Karina
- Pirana, Sulene
- Mendes, Beatriz C A
- Yengo, Christopher M
- Kachar, Bechara
- Mingroni-Netto, Regina C
Producer: 20191009
In:
Scientific reports vol. 8
Availability: No items available.
|
|
|
18.
|
AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations. [electronic resource] by
- Angeli, Claudia B
- Capelli, Leonardo P
- Auricchio, Maria Teresa B M
- Leal-Mesquita, Emygdya R
- Ribeiro-dos-Santos, Andrea K C
- Ferrari, Iris
- Oliveira, Silviene F
- Klautau-Guimarães, Maria de Nazaré
- Vianna-Morgante, Angela M
- Mingroni-Netto, Regina C
Producer: 20050418
In:
American journal of medical genetics. Part A vol. 132A
Availability: No items available.
|
|
|
19.
|
Patients with a Kabuki syndrome phenotype demonstrate DNA methylation abnormalities. [electronic resource] by
- Sobreira, Nara
- Brucato, Martha
- Zhang, Li
- Ladd-Acosta, Christine
- Ongaco, Chrissie
- Romm, Jane
- Doheny, Kimberly F
- Mingroni-Netto, Regina C
- Bertola, Debora
- Kim, Chong A
- Perez, Ana Ba
- Melaragno, Maria I
- Valle, David
- Meloni, Vera A
- Bjornsson, Hans T
Producer: 20180723
In:
European journal of human genetics : EJHG vol. 25
Availability: No items available.
|
|
|
20.
|
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. [electronic resource] by
- Lezirovitz, Karina
- Vieira-Silva, Gleiciele A
- Batissoco, Ana C
- Levy, Débora
- Kitajima, Joao P
- Trouillet, Alix
- Ouyang, Ellen
- Zebarjadi, Navid
- Sampaio-Silva, Juliana
- Pedroso-Campos, Vinicius
- Nascimento, Larissa R
- Sonoda, Cindy Y
- Borges, Vinícius M
- Vasconcelos, Laura G
- Beck, Roberto M O
- Grasel, Signe S
- Jagger, Daniel J
- Grillet, Nicolas
- Bento, Ricardo F
- Mingroni-Netto, Regina C
- Oiticica, Jeanne
Producer: 20210812
In:
Human molecular genetics vol. 29
Availability: No items available.
|