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Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome. [electronic resource] by
- Yeh, Erika
- Fanganiello, Roberto D
- Sunaga, Daniele Y
- Zhou, Xueyan
- Holmes, Gregory
- Rocha, Katia M
- Alonso, Nivaldo
- Matushita, Hamilton
- Wang, Yingli
- Jabs, Ethylin W
- Passos-Bueno, Maria Rita
Producer: 20131104
In:
PloS one vol. 8
Availability: No items available.
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Fibroblast growth factor 2 restrains Ras-driven proliferation of malignant cells by triggering RhoA-mediated senescence. [electronic resource] by
- Costa, Erico T
- Forti, Fábio L
- Matos, Tatiana G F
- Dermargos, Alexandre
- Nakano, Fábio
- Salotti, Jacqueline
- Rocha, Kátia M
- Asprino, Paula F
- Yoshihara, Celina K
- Koga, Marianna M
- Armelin, Hugo A
Producer: 20080908
In:
Cancer research vol. 68
Availability: No items available.
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Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? [electronic resource] by
- Jehee, Fernanda Sarquis
- Burin, Beatriz A
- Rocha, Kátia M
- Zechi-Ceide, Roseli
- Bueno, Daniela F
- Brito, Luciano
- Souza, Josiane
- Leal, Gabriela Ferraz
- Richieri-Costa, Antonio
- Alonso, Nivaldo
- Otto, Paulo A
- Passos-Bueno, Maria Rita
Producer: 20090730
In:
American journal of medical genetics. Part A vol. 149A
Availability: No items available.
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IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population. [electronic resource] by
- Brito, Luciano A
- Bassi, Camila F S
- Masotti, Cibele
- Malcher, Carolina
- Rocha, Kátia M
- Schlesinger, David
- Bueno, Daniela F
- Cruz, Lucas A
- Barbara, Ligia K
- Bertola, Débora R
- Meyer, Diogo
- Franco, Diogo
- Alonso, Nivaldo
- Passos-Bueno, Maria Rita
Producer: 20121109
In:
American journal of medical genetics. Part A vol. 158A
Availability: No items available.
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9.
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Genetic contribution for non-syndromic cleft lip with or without cleft palate (NS CL/P) in different regions of Brazil and implications for association studies. [electronic resource] by
- Brito, Luciano A
- Cruz, Lucas A
- Rocha, Kátia M
- Barbara, Ligia K
- Silva, Camila B F
- Bueno, Daniela F
- Aguena, Meire
- Bertola, Débora R
- Franco, Diogo
- Costa, André M
- Alonso, Nivaldo
- Otto, Paulo A
- Passos-Bueno, Maria Rita
Producer: 20111014
In:
American journal of medical genetics. Part A vol. 155A
Availability: No items available.
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Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy. [electronic resource] by
- Moreira, Danielle P
- Griesi-Oliveira, Karina
- Bossolani-Martins, Ana L
- Lourenço, Naila C V
- Takahashi, Vanessa N O
- da Rocha, Kátia M
- Moreira, Eloisa S
- Vadasz, Estevão
- Meira, Joanna Goes Castro
- Bertola, Debora
- O'Halloran, Eoghan
- Magalhães, Tiago R
- Fett-Conte, Agnes C
- Passos-Bueno, Maria Rita
Producer: 20150622
In:
PloS one vol. 9
Availability: No items available.
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Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies. [electronic resource] by
- Acuna-Hidalgo, Rocio
- Deriziotis, Pelagia
- Steehouwer, Marloes
- Gilissen, Christian
- Graham, Sarah A
- van Dam, Sipko
- Hoover-Fong, Julie
- Telegrafi, Aida B
- Destree, Anne
- Smigiel, Robert
- Lambie, Lindsday A
- Kayserili, Hülya
- Altunoglu, Umut
- Lapi, Elisabetta
- Uzielli, Maria Luisa
- Aracena, Mariana
- Nur, Banu G
- Mihci, Ercan
- Moreira, Lilia M A
- Borges Ferreira, Viviane
- Horovitz, Dafne D G
- da Rocha, Katia M
- Jezela-Stanek, Aleksandra
- Brooks, Alice S
- Reutter, Heiko
- Cohen, Julie S
- Fatemi, Ali
- Smitka, Martin
- Grebe, Theresa A
- Di Donato, Nataliya
- Deshpande, Charu
- Vandersteen, Anthony
- Marques Lourenço, Charles
- Dufke, Andreas
- Rossier, Eva
- Andre, Gwenaelle
- Baumer, Alessandra
- Spencer, Careni
- McGaughran, Julie
- Franke, Lude
- Veltman, Joris A
- De Vries, Bert B A
- Schinzel, Albert
- Fisher, Simon E
- Hoischen, Alexander
- van Bon, Bregje W
Producer: 20170607
In:
PLoS genetics vol. 13
Availability: No items available.
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