New insights reveal complex mechanisms involved in genomic imprinting.

由 Nicholls, R. D.
出版 1994

Three allele TaqI RFLP for probe 3-21 [D15S10] on chromosome 15q.

由 Nicholls, R D, Lalande, M
出版 1989

Diverse splicing mechanisms fuse the evolutionarily conserved bicistronic MOCS1A and MOCS1B open reading frames.

由 Gray, T A, Nicholls, R D
出版 2000

RFLPs for beta 2-microglobulin.

由 Nicholls, R D, Glatt, K, Latt, S A
出版 1989

Long range genome structure around the human alpha-globin complex analysed by PFGE.

由 Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
出版 1987

Unusual features of CpG-rich (HTF) islands in the human alpha globin complex: association with non-functional pseudogenes and presence within the 3' portion of the zeta gene.

由 Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
出版 1987

Reply to Engel

由 Knoll, J. H. M., Nicholls, R. D., Malcolm, S., Lalande, M.
出版 1991

Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichment.

由 Nicholls, R D, Hill, A V, Clegg, J B, Higgs, D R
出版 1985

Non-methylated CpG-rich islands at the human alpha-globin locus: implications for evolution of the alpha-globin pseudogene.

由 Bird, A P, Taggart, M H, Nicholls, R D, Higgs, D R
出版 1987

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

由 Knoll, J H, Glatt, K A, Nicholls, R D, Malcolm, S, Lalande, M
出版 1991

A model system to study genomic imprinting of human genes

由 Gabriel, J. M., Higgins, M. J., Gebuhr, T. C., Shows, T. B., Saitoh, S., Nicholls, R. D.
出版 1998

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

由 Nicholls, R D, Gottlieb, W, Russell, L B, Davda, M, Horsthemke, B, Rinchik, E M
出版 1993

Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster.

由 Jarman, A P, Nicholls, R D, Weatherall, D J, Clegg, J B, Higgs, D R
出版 1986

Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.

由 White, L. M., Rogan, P. K., Nicholls, R. D., Wu, B. L., Korf, B., Knoll, J. H.
出版 1996

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

由 Glenn, C. C., Saitoh, S., Jong, M. T., Filbrandt, M. M., Surti, U., Driscoll, D. J., Nicholls, R. D.
出版 1996

Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor.

由 Culiat, C T, Stubbs, L, Nicholls, R D, Montgomery, C S, Russell, L B, Johnson, D K, Rinchik, E M
出版 1993

Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.

由 Knoll, J H, Nicholls, R D, Magenis, R E, Glatt, K, Graham, J M, Kaplan, L, Lalande, M
出版 1990

High resolution gene mapping of the human alpha globin locus.

由 Nicholls, R D, Jonasson, J A, McGee, J O, Patil, S, Ionasescu, V V, Weatherall, D J, Higgs, D R
出版 1987

The mechanisms involved in formation of deletions and duplications of 15q11-q13.

由 Robinson, W P, Dutly, F, Nicholls, R D, Bernasconi, F, Peñaherrera, M, Michaelis, R C, Abeliovich, D, Schinzel, A A
出版 1998

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.

由 Ohta, T, Buiting, K, Kokkonen, H, McCandless, S, Heeger, S, Leisti, H, Driscoll, D J, Cassidy, S B, Horsthemke, B, Nicholls, R D
出版 1999