Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

Susan L. Christian, Wendy P. Robinson, Binquan Huang et al. · PubMed · 1995 · 189 citations

Life Sciences, Molecular Genetics, Molecular Medicine +7

A somatic origin of homologous Robertsonian translocations and isochromosomes

Wendy P. Robinson, Memnune Yüksel‐Apak, Giovanni Neri et al. · PubMed · 1994 · 129 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

Faye A. Eggerding, S. A. Schonberg, FF Chehab et al. · PubMed · 1994 · 91 citations

Medicine, Genetics, Pediatrics +11

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

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

Isabel Lorda‐Sánchez, Franz Binkert, Marco Maechler et al. · PubMed · 1991 · 43 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16