Parental origin and mechanism of formation of X chromosome structural abnormalities: Four cases determined with RFLPs

Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome

Robert D. Nicholls, Joan H.M. Knoll, Merlin G. Butler et al. · Nature · 1989 · 887 citations

Life Sciences, Genetics, Molecular Genetics +11

Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)

Kay E. Davies, Jean‐Louis Mandel, Anthony P. Monaco et al. · Cytogenetics and Cell Genetics · 2008 · 593 citations

Life Sciences, Genetics, Molecular Genetics +12

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

Joan H.M. Knoll, Robert D. Nicholls, R.E. Magenis et al. · American Journal of Medical Genetics · 1989 · 583 citations

Life Sciences, Genetics, Molecular Genetics +17

The Cytogenetics of Mammalian Autosomal Rearrangements

Susan Roberts · Journal of Medical Genetics · 1989 · 392 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Cytogenetic and molecular analysis of sex-chromosome monosomy.

Terry Hassold, Frances Benham, Mark Leppert · PubMed · 1988 · 155 citations

Life Sciences, Genetics, Molecular Genetics +14