A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation

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

A molecular genetic approach to the identification of isochromosomes of chromosome 21

LisaG. Shaffer, ColleenK. Jackson-Cook, JoanneM. Meyer et al. · Human Genetics · 1991 · 129 citations

Life Sciences, Genetics, Molecular Genetics +10

A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome

P. A. Jacobs, P R Betts, Annette E. Cockwell et al. · Annals of Human Genetics · 1990 · 108 citations

Life Sciences, Genetics, Molecular Genetics +15

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22

Neil J. Fraser, Yvonne Boyd, Ian Craig · Genomics · 1989 · 90 citations

Life Sciences, Genetics, Molecular Genetics +6

Analysis of DNA polymorphisms suggests that most de novo dup(21q) chromosomes in patients with Down syndrome are isochromosomes and not translocations

Stylianos E. Antonarakis, P A Adelsberger, Michael B. Petersen et al. · PubMed · 1990 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11