Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies MV Gomes, J Huber, RA Ferriani, AM Amaral Neto, ES Ramos Molecular human reproduction 15 (8), 471-477, 2009 | 139 | 2009 |
The P48T germline mutation and polymorphism in the CDKN2A gene of patients with melanoma J Huber, ES Ramos Brazilian journal of medical and biological research 39, 237-241, 2006 | 26 | 2006 |
Fuhrmann syndrome: two Brazilian cases J Huber, JB Volpon, ES Ramos Clinical Dysmorphology 12 (2), 85-88, 2003 | 24 | 2003 |
The epidemiology of sepsis in paediatric intensive care units in Brazil (the Sepsis PREvalence Assessment Database in Pediatric population, SPREAD PED): an observational study DC de Souza, JG Martin, VS Lanziotti, CF de Oliveira, C Tonial, ... The Lancet Child & Adolescent Health 5 (12), 873-881, 2021 | 22 | 2021 |
Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature AC Laus, WAR Baratela, LAF Laureano, SA Santos, J Huber, ES Ramos, ... American Journal of Medical Genetics Part A 158 (4), 821-827, 2012 | 15 | 2012 |
Investigation of IGF2/ApaI and H19/RsaI polymorphisms in patients with cutaneous melanoma MR Soares, J Huber, AFL Rios, ES Ramos Growth Hormone & IGF Research 20 (4), 295-297, 2010 | 15 | 2010 |
Ambulatório de genética médica na Apae: experiência no ensino médico de graduação DG Melo, MMP Demarzo, J Huber Revista Brasileira de Educação Médica 32, 396-402, 2008 | 10 | 2008 |
Oral rehabilitation of a child with hypohidrotic ectodermal dysplasia CP Torres, AC Dos Reis, AM Queiroz, MB Stuani, P Mira, PS Ferreira, ... Journal of Dentistry for Children 86 (3), 158-163, 2019 | 8 | 2019 |
Anomalias congênitas: validade das informações das declarações de nascido vivo em uma maternidade de Ribeirão Preto, São Paulo CUB de Mauá Pediatria (São Paulo) 30 (3), 159-164, 2008 | 8 | 2008 |
Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations LF Araujo, GA Molfetta, OC Vincenzi, J Huber, LA Teixeira, VE Ferraz, ... The International Journal of Biological Markers 34 (1), 80-89, 2019 | 7 | 2019 |
Development and freezability of bovine embryos cultured in bovine oviducts for seven days V Havlicek, S Cseh, A Kuzmany, J Huber, H Pothmann-Reichl, ... REPRODUCTION IN DOMESTIC ANIMALS 42, 101-102, 2007 | 2 | 2007 |
Velocardiofacial syndrome with a rare t (2; 22) J Huber, CA Rainho, MV Gomes, SA Santos, ES Ramos Clinical Dysmorphology 16 (3), 181-183, 2007 | 1 | 2007 |
Effect of culture conditions on the cryo-tolerance of bovine embryos V Havlicek, S Cseh, M Dobretsberger, J Huber, U Besenfelder REPRODUCTION IN DOMESTIC ANIMALS 41 (4), 305-305, 2006 | 1 | 2006 |
DE NO/O) COMPLEX (CHROMOSOME REARRANGEMENT: A STUDY OF TWO PATIENTS DG MEL, J Huber, LR Giuliani, LE MAZZUCATTO, M Riegel Genetic counseling 15 (3), 303-310, 2004 | 1 | 2004 |
Increased insulin-like growth factor 1 and interferon tau signaling in pregnant cows with an extended voluntary waiting period of 120 days C Gabler, S Widera, J Huber, C Holder, L Jessen, K Mense, M Jung, ... REPRODUCTION IN DOMESTIC ANIMALS 57, 9-9, 2022 | | 2022 |
Higher mRNA expression of selected pro-inflammatory factors on day 1 after artificial insemination in cows which conceived S Widera, J Huber, C Holder, L Jessen, K Mense, M Jung, C Gabler REPRODUCTION IN DOMESTIC ANIMALS 55, 34-34, 2020 | | 2020 |
Genitopatellar syndrome: case report CGP Albuquerque, RE Maia, TTSL Cavalcanti, J Huber, ES Ramos Resumos, 2017 | | 2017 |
Familial non-disjunction and segregation variation of a supernumerary marker chromosome 15 in members of a large family TM Joaquim, DC de Souza, CHP Grangeiro, J Huber, AC Laus, ... Abstracts, 2017 | | 2017 |
High resolution array-CGH analysis apparently balanced translocations reveals complex chromosomal rearrangement and cryptic deletions associated with the phenotypes TM Joaquim, CHP Grangeiro, FG de Oliveira Gennaro, ... Semina: Ciências Biológicas e da Saúde 38 (1supl), 183-183, 2017 | | 2017 |
Caracterização molecular da polipose adenomatosa familial na região sudeste do Brasil: descrição de nove mutações novas GA Molfetta, OC Vincenzi, J Huber, VEF Ferraz, WA Silva Júnior Trabalhos apresentados, 2015 | | 2015 |