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American Journal of Medical Genetics. Part A|May 14, 2011
Additional features of unique Primrose syndrome phenotypeDaniel Rocha Carvalho, Carlos Eduardo Speck-Martins
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|March 23, 2011
Craniofacial findings in fibrodysplasia ossificans progressiva: computerized tomography evaluationDaniel Rocha Carvalho, Luciano Farage, Bernardo Jose Alves Ferreira Martins, et al.
American Journal of Medical Genetics. Part A|September 28, 2011
Tibial hemimelia in Langer-Giedion syndrome with 8q23.1-q24.12 interstitial deletionDaniel Rocha Carvalho, Savana Camilla Lima Santos, Maria Dulce Valverde Oliveira, et al.
Gene|September 11, 2012
Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytesDaniel Rocha Carvalho, Guilherme Dotto Brand, Jaime Moritz Brum, et al.
American Journal of Medical Genetics. Part A|August 3, 2018
Femoral-facial syndrome: A review of the literature and 14 additional patients including a monozygotic discordant twin pairMaria Dora Jazmin Lacarrubba-Flores, Daniel Rocha Carvalho, Erlane Marques Ribeiro, et al.
European Journal of Medical Genetics|May 31, 2020
Unique skeletal manifestations in patients with Primrose syndromeVeronica Arora, Eyby Leon, Jullianne Diaz, et al.
Molecular Genetics and Metabolism|July 1, 2023
Phenotypic, molecular, and functional characterization of COQ7-related primary CoQ10 deficiency: Hypomorphic variants and two distinct disease entitiesParith Wongkittichote, Maria Laura Duque Lasio, Martina Magistrati, et al.
Modern Rheumatology|July 25, 2023
Czech dysplasia mimicking rheumatoid arthritis: Case series and literature reviewLarissa Aniceto Moreira, Daniel Rocha Carvalho, Savana Camilla Lima Santos, et al.
Nature|February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulatorLila Allou, Sara Balzano, Andreas Magg, et al.
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