Mapping and complex expression pattern of the human NPAP60L nucleoporin gene
TRICHET, V, SHKOLNY, D, DUNHAM, I, BEARE, D, MCDERMID, H. E
Published in Cytogenetics and cell genetics (01.01.1999)
Published in Cytogenetics and cell genetics (01.01.1999)
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Mutation analysis of Drosophila dikar/CG32394, homologue of the chromatin-remodelling gene CECR2
Keuling, A, Yang, F, Hanna, S, Wang, H, Tully, T, Burnham, A, Locke, J, McDermid, H.E
Published in Genome (2008)
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Published in Genome (2008)
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Cat eye syndrome chromosome breakpoint clustering : identification of two intervals also associated with 22q11 deletion syndrome breakpoints
MCTAGGART, K. E, BUDARF, M. L, DRISCOLL, D. A, EMANUEL, B. S, FERREIRA, P, MCDERMID, H. E
Published in Cytogenetic and genome research (01.01.1998)
Published in Cytogenetic and genome research (01.01.1998)
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Conference Proceeding
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Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13. 3
Nesslinger, N.J., McDermid, H.E., Gorski, J.L., Kurczynski, T.W., French, B.N., Shapira, S.K., Siegel-Bartelt, J., Dumanski, J.P., Cullen, R.F. Jr
Published in American journal of human genetics (01.03.1994)
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Published in American journal of human genetics (01.03.1994)
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A polymorphic locus, D10S5, at 10q21.1
MCDERMID, H. E, GOODFELLOW, P. J, DUNCAN, A. M. V, BRASCH, K. R, SIMPSON, N. E, SOUZA, C. D, HOLDEN, J. J. A, WHITE, B. N
Published in Nucleic acids research (10.07.1987)
Published in Nucleic acids research (10.07.1987)
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