The Gravity Field of the Saturnian System from Satellite Observations and Spacecraft Tracking Data
Jacobson, R. A, Antreasian, P. G, Bordi, J. J, Criddle, K. E, Ionasescu, R, Jones, J. B, Mackenzie, R. A, Meek, M. C, Parcher, D, Pelletier, F. J, Owen, Jr., W. M, Roth, D. C, Roundhill, I. M, Stauch, J. R
Published in The Astronomical journal (01.12.2006)
Published in The Astronomical journal (01.12.2006)
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Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy
Ionasescu, V V, Searby, C, Ionasescu, R, Neuhaus, I M, Werner, R
Published in Neurology (01.08.1996)
Published in Neurology (01.08.1996)
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New point mutations and deletions of the connexin 32 gene in x-linked charcot-marie-tooth neuropathy
Ionasescu, V., Searby, Ch, Ionasescu, R., Meschino, W.
Published in Neuromuscular disorders : NMD (01.07.1995)
Published in Neuromuscular disorders : NMD (01.07.1995)
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Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy
Ionasescu, V V, Trofatter, J, Haines, J L, Ionasescu, R, Searby, C
Published in Neurology (01.04.1992)
Published in Neurology (01.04.1992)
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Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1
Pericak-Vance, M A, Barker, D F, Bergoffen, J A, Chance, P, Cochrane, S, Dahl, N, Exler, M C, Fain, P R, Fairweather, N D, Fischbeck, K
Published in Human heredity (01.05.1995)
Published in Human heredity (01.05.1995)
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Linkage between the loci for Duffy (FY) and serum amyloid P component (APCS) on human chromosome 1
Ionasescu, V, Burns, T, Searby, C, Ionasescu, R
Published in Cytogenetics and cell genetics (01.01.1987)
Published in Cytogenetics and cell genetics (01.01.1987)
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Recombinant DNA study of Duchenne muscular dystrophy occurring in a myotonic dystrophy family
Ionasescu, V, Searby, C, Ionasescu, R, Burns, T
Published in Acta neurologica Scandinavica (01.05.1988)
Published in Acta neurologica Scandinavica (01.05.1988)
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Inherited ophthalmoplegia with intestinal pseudo-obstruction
Ionasescu, V., Thompson, S.H., Ionasescu, R., Searby, Ch, Anuras, S., Christensen, J., Mitros, F., Hart, M., Bosch, P.
Published in Journal of the neurological sciences (01.01.1983)
Published in Journal of the neurological sciences (01.01.1983)
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Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1
Ionasescu, V, Burns, T, Searby, C, Ionasescu, R, Whitehead, A S
Published in Cytogenetics and cell genetics (01.01.1988)
Published in Cytogenetics and cell genetics (01.01.1988)
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Charcot-Marie-Tooth neuropathy related to chromosome 1
Ionasescu, V V, Trofatter, J, Haines, J L, Ionasescu, R, Searby, C
Published in American journal of medical genetics (01.03.1992)
Published in American journal of medical genetics (01.03.1992)
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Alterations in creatine kinase in fresh muscle and cell cultures in Duchenne dystrophy
Ionasescu, V, Ionasescu, R, Feld, R, Witte, D, Cancilla, P, Kaeding, L, Stern, L Z
Published in Annals of neurology (01.04.1981)
Published in Annals of neurology (01.04.1981)
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