Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil
Gheno, T. C., Furtado, G. V., Saute, J. A. M., Donis, K. C., Fontanari, A. M. V., Emmel, V. E., Pedroso, J. L., Barsottini, O., Godeiro‐Junior, C., Linden, H., Ternes Pereira, E., Cintra, V. P., Marques, W., Castilhos, R. M., Alonso, I., Sequeiros, J., Cornejo‐Olivas, M., Mazzetti, P., Leotti, V. B., Jardim, L. B., Saraiva‐Pereira, M. L.
Published in European journal of neurology (01.07.2017)
Published in European journal of neurology (01.07.2017)
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Klippel–Trenaunay–Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis
Gonçalves, L. F., Muñoz Rojas, M. V., Vitorello, D., Ternes Pereira, E., Pereima, M., Saab Neto, J. A.
Published in Ultrasound in obstetrics & gynecology (01.06.2000)
Published in Ultrasound in obstetrics & gynecology (01.06.2000)
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Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
AFZAL, A. R, RAJAB, A, FENSKE, C, CROSBY, A, LAHIRI, N, TERNES-PEREIRA, E, MURDAY, V. A, HOULSTON, R, PATTON, M. A, JEFFERY, S
Published in Human genetics (01.03.2000)
Published in Human genetics (01.03.2000)
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Novel mutations in the 3' region of the polycystic kidney disease 1 (PKD1) gene
AFZAL, A. R, HAND, M, TERNES-PEREIRA, E, SAGGAR-MALIK, A, TAYLOR, R, JEFFERY, S
Published in Human genetics (01.12.1999)
Published in Human genetics (01.12.1999)
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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2
Jeffery, Steve, Afzal, Ali R, Rajab, Anna, Fenske, Christiane D, Oldridge, Michael, Elanko, Navaratnam, Ternes-Pereira, Eliana, Tüysüz, Beyhan, Murday, Victoria A, Patton, Michael A, Wilkie, Andrew O.M
Published in Nature genetics (01.08.2000)
Published in Nature genetics (01.08.2000)
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Journal Article
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22
Afzal, A.R., Rajab, A., Fenske, C., Crosby, A., Lahiri, N., Ternes-Pereira, E., Murday, V.A., Houlston, R., Patton, M.A., Jeffery, S.
Published in Human genetics (01.03.2000)
Published in Human genetics (01.03.2000)
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