Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith–Wiedemann syndrome and ovarian steroid cell tumour

The clinical phenotype of mosaicism for genome‐wide paternal uniparental disomy: Two new reports

Meredith Wilson, Gregory B. Peters, Bruce Bennetts et al. · American Journal of Medical Genetics Part A · 2007 · 142 citations

Life Sciences, Genetics, Molecular Genetics +16

H19, a marker of developmental transition, is reexpressed in human atherosclerotic plaques and is regulated by the insulin family of growth factors in cultured rabbit smooth muscle cells.

David K. Han, Zin Z. Khaing, Richard A. Pollock et al. · Journal of Clinical Investigation · 1996 · 98 citations · Full text

Life Sciences, Developmental Biology, Molecular Biology +16

Androgenetic/Biparental Mosaicism in an Infant with Hepatic Mesenchymal Hamartoma and Placental Mesenchymal Dysplasia

Robyn C. Reed, Linda Beischel, Jonathan Schoof et al. · Pediatric and Developmental Pathology · 2008 · 54 citations

Life Sciences, Genetics, Molecular Genetics +17

Genomic Imprinting and the Endometrial Cycle

I. Ariel, Daniel C. Weinstein, Raimo Voutilainen et al. · Diagnostic Molecular Pathology · 1997 · 53 citations

Life Sciences, Genetics, Molecular Biology +12

Genome-wide loss of maternal alleles in a nephrogenic rest and Wilms' tumour from a BWS patient

PaulR. Hoban, Jim Heighway, G White et al. · Human Genetics · 1995 · 38 citations

Life Sciences, Genetics, Molecular Genetics +17