subject area of
- Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia Journal Articles
- Prader–Willi syndrome and Tay–Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq Journal Articles
- Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell???Silver syndrome? Journal Articles
- Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15 Journal Articles
- Trisomy 22 Mosaicism and Normal Developmental Outcome: Report of Two Patients and Review of the Literature Journal Articles