Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
Becher, Mark W, Morrison, Leslie, Davis, Larry E, Maki, Wusi C, King, Molly K, Bicknell, Joseph M, Reinert, Brian L, Bartolo, Claire, Bear, David G
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Published in JAMA : the journal of the American Medical Association (21.11.2001)
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Spectrum of small mutations in the dystrophin coding region
PRIOR, T. W, BARTOLO, C, PEARL, D. K, PAPP, A. C, SNYDER, P. J, SEDRA, M. S, BURGHES, A. H. M, MENDELL, J. R
Published in American journal of human genetics (01.07.1995)
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Published in American journal of human genetics (01.07.1995)
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Comparison of capillary electrophoresis and polyacrylamide gel electrophoresis for the evaluation of T and B cell clonality by polymerase chain reaction
Beaubier, N T, Hart, A P, Bartolo, C, Willman, C L, Viswanatha, D S
Published in Diagnostic molecular pathology (01.09.2000)
Published in Diagnostic molecular pathology (01.09.2000)
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Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy
Bartolo, C, McAndrew, P E, Sosolik, R C, Cawley, K A, Balcerzak, S P, Brandt, J T, Prior, T W
Published in Archives of pathology & laboratory medicine (1976) (01.07.1998)
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Published in Archives of pathology & laboratory medicine (1976) (01.07.1998)
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A novel splice site mutation in a Becker muscular dystrophy patient
Bartolo, C, Papp, A C, Snyder, P J, Sedra, M S, Burghes, A H, Hall, C D, Mendell, J R, Prior, T W
Published in Journal of medical genetics (01.04.1996)
Published in Journal of medical genetics (01.04.1996)
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Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16
Prior, T W, Bartolo, C, Papp, A C, Snyder, P J, Sedra, M S, Burghes, A H, Mendell, J R
Published in Human molecular genetics (01.07.1994)
Published in Human molecular genetics (01.07.1994)
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