New insights reveal complex mechanisms involved in genomic imprinting.

le Nicholls, R. D.
Foilsithe 1994

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

le Nicholls, R D, Lalande, M
Foilsithe 1989

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

le Gray, T A, Nicholls, R D
Foilsithe 2000

RFLPs for beta 2-microglobulin.

le Nicholls, R D, Glatt, K, Latt, S A
Foilsithe 1989

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

le Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
Foilsithe 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.

le Fischel-Ghodsian, N, Nicholls, R D, Higgs, D R
Foilsithe 1987

Reply to Engel

le Knoll, J. H. M., Nicholls, R. D., Malcolm, S., Lalande, M.
Foilsithe 1991

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

le Nicholls, R D, Hill, A V, Clegg, J B, Higgs, D R
Foilsithe 1985

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

le Bird, A P, Taggart, M H, Nicholls, R D, Higgs, D R
Foilsithe 1987

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

le Knoll, J H, Glatt, K A, Nicholls, R D, Malcolm, S, Lalande, M
Foilsithe 1991

A model system to study genomic imprinting of human genes

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

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

le Nicholls, R D, Gottlieb, W, Russell, L B, Davda, M, Horsthemke, B, Rinchik, E M
Foilsithe 1993

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

le Jarman, A P, Nicholls, R D, Weatherall, D J, Clegg, J B, Higgs, D R
Foilsithe 1986

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

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

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

le Glenn, C. C., Saitoh, S., Jong, M. T., Filbrandt, M. M., Surti, U., Driscoll, D. J., Nicholls, R. D.
Foilsithe 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.

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

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

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

High resolution gene mapping of the human alpha globin locus.

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

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

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

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

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