Renal dysfunction, rod‐cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B
Roberts, Lisa, Julius, Stephanie, Dawlat, Shrinav, Yildiz, Safiye, Rebello, George, Meldau, Surita, Pillay, Komala, Esterhuizen, Alina, Vorster, Alvera, Benefeld, Gameda, Rocha, Jorge, Beighton, Peter, Sellars, Sean L., Thandrayen, Kebashni, Pettifor, John M., Ramesar, Raj S.
Published in Human mutation (01.11.2020)
Published in Human mutation (01.11.2020)
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An evaluation of the Shandon Papspin liquid-based oral test using a novel cytologic scoring system
Afrogheh, Amir, DDS, MChD, Wright, Colleen Anne, MD, MMed, FCPath, FRCPath, FIAC, PhD, Sellars, Sean Liam, MD, FRCS, FCS, FACS, Wetter, Julie, MD, MMed, FCRadOnc, Pelser, Andrew, MD, MRCS, Schubert, Pawel Tomasz, MD, MMed, FCPath, MIAC, Hille, Jos, DDS, MDent, FCPath
Published in Oral surgery, oral medicine, oral pathology and oral radiology (01.06.2012)
Published in Oral surgery, oral medicine, oral pathology and oral radiology (01.06.2012)
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Tributes
Sellars, Sean L, Hamersma, Herman, Kozlowski, Kazimierz, Winship, Ingrid, Medefindt, Claudette, Zieff, Sol, Bonafede, Peter, Gericke, George, Viljoen, Denis L
Published in South African medical journal (25.05.2016)
Published in South African medical journal (25.05.2016)
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Tracheoesophageal Speech in a Developing World Community
Fagan, Johannes J, Lentin, Roslyn, Oyarzabal, Manuel F, Isaacs, Sedick, Sellars, Sean L
Published in Archives of otolaryngology--head & neck surgery (01.01.2002)
Published in Archives of otolaryngology--head & neck surgery (01.01.2002)
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Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK
Reichenberger, Ernst, Tiziani, Valdenize, Watanabe, Shoji, Park, Lucy, Ueki, Yasuyoshi, Santanna, Carla, Baur, Scott T., Shiang, Rita, Grange, Dorothy K., Beighton, Peter, Gardner, Jessica, Hamersma, Herman, Sellars, Sean, Ramesar, Rajkumar, Lidral, Andrew C., Sommer, Annmarie, Raposo do Amaral, Cassio M., Gorlin, Robert J., Mulliken, John B., Olsen, Bjorn R.
Published in American journal of human genetics (01.06.2001)
Published in American journal of human genetics (01.06.2001)
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A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African family
Butt, J, Greenberg, J, Winship, I, Sellars, S, Beighton, P, Ramesar, R
Published in Human molecular genetics (01.01.1994)
Published in Human molecular genetics (01.01.1994)
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Hearing impairment and pigmentary disturbance
Beighton, P, Ramesar, R, Winship, I, Viljoen, D, Greenberg, J, Young, K, Curtis, D, Sellars, S
Published in Annals of the New York Academy of Sciences (01.01.1991)
Published in Annals of the New York Academy of Sciences (01.01.1991)
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Congenital cerebrospinal fluid fistula through the inner ear and meningitis
Phelps, P D, Proops, D, Sellars, S, Evans, J, Michaels, L
Published in Journal of laryngology and otology (01.06.1993)
Published in Journal of laryngology and otology (01.06.1993)
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Rod-cone dystrophy, sensorineural deafness, and renal dysfunction: an autosomal recessive syndrome?
Beighton, P, Bartmann, L, Bingham, G, Sellars, S
Published in American journal of medical genetics (01.11.1993)
Published in American journal of medical genetics (01.11.1993)
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