| Ano | Produção | Detalhes |
|---|
| 2013 | MATTOS, V. F. ; ROMANO, M. A. ; BENCKE, J. C. ; POLLI, J. B. ; ROSA, R. C. M. ; ROSA, A. F. M. ; POGUE, R. ; BACIL, M. L. ; MUSA, S. H. ; ZEN, P. R. G.. Relato de uma menina apresentando aplasia fibular, campomelia tibial e oligossindactilia: síndrome FATCO. 2013. | |
| 2012 | CUNHA, I. R. C. ; MARQUES, F. A. ; MEDINA, C. T. N. ; CARDOSO, M. T. O. ; POGUE, R.. Caracterização clínica e molecular de pacientes com baixa estatura na região Centro-Oeste para estabelecimento de protocolo de tratamento.. 2012. | |
| 2012 | GARCIA, G. E. M. ; NASCIMENTO, A. K. ; Pogue, R.. Imprinting Genômico. 2012. | |
| 2012 | GARCIA, G. E. M. ; NASCIMENTO, A. K. ; Pogue, R.. Síndrome de Angelman e Imprinting Genômico. 2012. | |
| 2012 | HEREDIA, R. S. ; Neves CT ; CARDOSO, T. ; CANO, T. M. ; CORDOBA, M. ; ARAUJO, R. O. ; POGUE, R.. .ESTUDO DE DELEÇÃO INTERSTICIAL 6q POR CHG-ARRAY: RELATO DE CASO. 2012. | |
| 2012 | NASCIMENTO, A. K. ; CANABRAVA, L. E. ; GARCIA, G. E. M. ; Pogue, R.. Síndrome de Silver Russell. 2012. | |
| 2012 | NASCIMENTO, A. K. ; GARCIA, G. E. M. ; Pogue, R.. Síndrome de Prader-Willi. 2012. | |
| 2011 | POGUE, R.. Exome Sequencing.. 2011. | |
| 2007 | POGUE, R. ; Bibikova, E ; Brugger, S ; Retting, K ; Lyons, K. The Type I BMP receptor- ActR1 is important in vertebral development, and shows functional redundancy with Bmpr1a and Bmpr1b.. 2007. | |
| 2004 | POGUE, R. ; Ehtesham, N ; Repetto, G ; Carrero-Valenzuela, R ; Bazan de Casella, C ; de Pons, S ; Cormier-Darre, V ; Cohn, D. A recurrent mutation in the Dyggve-Melchior-Clausen/Smith-McCort dysplasia disease gene identified in families from Guam, Argentina and Chile.. 2004. | |
| 2003 | POGUE, R. ; Sebald, E ; King, L ; Day, A ; Castro, F ; Kronstadt, E ; Nelson, S ; Krakow, D ; Cohn, D. Characterization of the gene-expression profile of human fetal cartilage.. 2003. | |
| 2002 | Krakow, D ; Sebald, E ; POGUE, R. ; Cohn, D. Use of cartilage cDNA microarrays to dissect the molecular pathways in thanatophoric and campomelic dysplasias.. 2002. | |
| 2002 | POGUE, R. ; Sebald, E ; Cohn, D ; Krakow, D. Identification of novel cartilage-expressed genes.. 2002. | |
| 1999 | POGUE, R. ; Pollitt, C ; Davison, K ; Moss, JA ; Pyle, A ; Bushby, K ; Anderson, LV. Molecular examination of muscle from limb-girdle muscular dystrophy type 2A patients.. 1999. | |
| 1998 | Anderson, LV ; POGUE, R. ; Pollitt, C ; Bushby, K. Monoclonal antibodies to calpain 3 and protein expression in patients with limb-girdle muscular dystrophy type 2A (LGMD 2A).. 1998. | |
| 1998 | POGUE, R. ; Anderson, LV ; Pollitt, C ; Bushby, K. An integrated approach to the molecular analysis of the sarcoglycanopathies.. 1998. | |
| 1997 | POGUE, R. ; West, S ; Bushby, K. A modification of the single-strand conformational analysis technique for large scale mutation analysis. HUGO convention on mutation detection. 1997. | |
| 1996 | POGUE, R. ; Bushby, K. Mutation detection in the limb-girdle muscular dystrophies.. 1996. | |
