R D Nicholls

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.

R. Nicholls, R D Nicholls, J L Knepper, 2001, Annual review of genomics and human genetics.

Angelman and Prader-Willi syndrome: a magnetic resonance imaging study of differences in cerebral structure.

J C Honeyman, E V Staab, C. Leonard, 1993, American journal of medical genetics.

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

A. Bird, D. Higgs, R. Nicholls, 1987, The EMBO journal.

Phylogenetic conservation of the makorin-2 gene, encoding a multiple zinc-finger protein, antisense to the RAF1 proto-oncogene.

T A Gray, R. Nicholls, T. Gray, 2001, Genomics.

An imprinted, mammalian bicistronic transcript encodes two independent proteins.

T A Gray, S. Saitoh, R. Nicholls, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.

M. Nöthen, H. Smeets, A. V. D. van den Ouweland, 1998, American journal of human genetics.

Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center.

T A Gray, J. Greally, R. Nicholls, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Imprinting in Prader-Willi and Angelman syndromes.

S. Saitoh, B. Horsthemke, R. Nicholls, 1998, Trends in genetics : TIG.

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.

S. Latt, J. Opitz, J. Graham, 1989, American journal of medical genetics.

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

D. J. Driscoll, D. Theriaque, C. Williams, 2001, Journal of medical genetics.