Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease
Kandt, R. S, Haines, J. L, Smith, M, Northrup, H, Gardner, R. J. M, Short, M. P, Dumars, K, Roach, E. S, Steingold, S, Wall, S, Blanton, S. H, Flodman, P, Kwiatkowski, D. J, Jewell, A, Weber, J. L, Roses, A. D, Pericak-Vance, M. A
Published in Nature genetics (01.09.1992)
Published in Nature genetics (01.09.1992)
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Journal Article
Mutation analysis of the TSC2 gene in an African-American family
Kumar, A, Kandt, R S, Wolpert, C, Roses, A D, Pericak-Vance, M A, Gilbert, J R
Published in Human molecular genetics (01.12.1995)
Published in Human molecular genetics (01.12.1995)
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Journal Article
A novel splice site mutation (156 + 1G→A) in the TSC2 gene
Kumar, A, Kandt, RS, Wolpert, C, Roses, AD, Pericak-Vance, MA, Gilbert, JR
Published in Human mutation (1997)
Published in Human mutation (1997)
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Journal Article
18‐FLUORODEOXYGLUCOSE POSITRON EMISSION TOMOGRAPHY IN CHILDREN AND ADOLESCENTS WITH TRAUMATIC BRAIN INJURY
Worley, Gordon, Hoffman, John M., Paine, Susan S., Kalman, Sophia L., Claerhout, Susan J., Boyko, Orest B., Kandt, Raymond S., Santos, Cesar C., Hanson, Michael W., Oakes, W. Jerry, Coleman, R. Edward
Published in Developmental medicine and child neurology (01.03.1995)
Published in Developmental medicine and child neurology (01.03.1995)
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Journal Article
A de novo frame-shift mutation in the tuberin gene
Kumar, A, Wolpert, C, Kandt, R S, Segal, J, Pufky, J, Roses, A D, Pericak-Vance, M A, Gilbert, J R
Published in Human molecular genetics (01.08.1995)
Published in Human molecular genetics (01.08.1995)
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Journal Article
Absence of linkage of ABO blood group locus to familial tuberous sclerosis
Kandt, R.S., Pericak-Vance, M.A., Hung, W.-Y., Gardner, R.J.M., Nellist, M., Phillips, K., Warner, K., Speer, M.C., Crossen, P.E., Laing, N.G., Roses, A.D.
Published in Experimental neurology (01.06.1989)
Published in Experimental neurology (01.06.1989)
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Journal Article
Duchenne muscular dystrophy: high frequency of deletions
Bartlett, R J, Pericak-Vance, M A, Koh, J, Yamaoka, L H, Chen, J C, Hung, W Y, Speer, M C, Wapenaar, M C, Van Ommen, G J, Bakker, E
Published in Neurology (01.01.1988)
Published in Neurology (01.01.1988)
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Journal Article
Mspl RFLP for microtubule associated protein-2 (MAP2)
ALBERTS, M. J, KANDT, R. S, PERICAK-VANCE, M. A, BEBOUT, J, SPEER, M. C, SIDDIQUE, T. S, YAMAOKA, L, HUNG, W.-Y, GASKELL, P. C, ROSES, A. D
Published in Nucleic acids research (25.02.1991)
Published in Nucleic acids research (25.02.1991)
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Journal Article
Prenatal detection of an inherited Duchenne muscular dystrophy deletion allele
Bartlett, R J, Pericak-Vance, M A, Lanman, Jr, J T, Killam, A P, Gilbert, J R, Stajick, J M, Chen, J C, Siddique, T, Kandt, R S, Sirotkin-Roses, M
Published in Neurology (01.02.1987)
Published in Neurology (01.02.1987)
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Hysterical conversion reactions mimicking neurological disease
Bangash, I H, Worley, G, Kandt, R S
Published in American journal of diseases of children (1960) (01.11.1988)
Published in American journal of diseases of children (1960) (01.11.1988)
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Hypertensive encephalopathy in children: neuroimaging and treatment
Kandt, R S, Caoili, A Q, Lorentz, W B, Elster, A D
Published in Journal of child neurology (01.05.1995)
Published in Journal of child neurology (01.05.1995)
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