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

Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci

(2012) Matthias Begemann et al.   Epigenetics

Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disorders

(2011) Thomas Eggermann et al.   Epigenomics

Beckwith-Wiedemann syndrome

(2010) Sanaa Choufani et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Androgenetic/biparental mosaicism in a girl with Beckwith–Wiedemann syndrome-like and upd(14)pat-like phenotypes

(2010) Kazuki Yamazawa et al.   JOURNAL OF HUMAN GENETICS

Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism

(2010) V. Romanelli et al.   JOURNAL OF MEDICAL GENETICS

Uniparental disomy in cancer

(2009) Musaffe Tuna et al.   TRENDS IN MOLECULAR MEDICINE

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

(2008) Robyn C. Reed et al.   PEDIATRIC AND DEVELOPMENTAL PATHOLOGY