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S. Kumar

Department of Genetics

Center for Hereditary and Communication Disorders

Boys Town National Research Hospital

Omaha

USA

[email]@boystown.org

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Affiliations

Department of Genetics, Center for Hereditary and Communication Disorders, Boys Town National Research Hospital, Omaha, USA. 1998 - 2000
Department of Genetics, Boys Town National Research Hospital, Omaha, Nebraska 68131, USA. 1996

References

Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications. Kumar, S., Deffenbacher, K., Marres, H.A., Cremers, C.W., Kimberling, W.J. Am. J. Hum. Genet. (2000) [Pubmed]
Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13. Kumar, S., Marres, H.A., Cremers, C.W., Kimberling, W.J. Am. J. Med. Genet. (1998) [Pubmed]
Identification of three novel mutations in human EYA1 protein associated with branchio-oto-renal syndrome. Kumar, S., Kimberling, W.J., Weston, M.D., Schaefer, B.G., Berg, M.A., Marres, H.A., Cremers, C.W. Hum. Mutat. (1998) [Pubmed]
Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q. Kumar, S., Kimberling, W.J., Lanyi, A., Sumegi, J., Pinnt, J., Ing, P., Tinley, S., Marres, H.A., Cremers, C.W. Genomics (1996) [Pubmed]