Beckwith–Wiedemann syndrome (BWS) is a model disorder for the study of imprinting,
growth dysregulation, and tumorigenesis. Unique observations in this disorder point to an …

Abstract The Beckwith–Wiedemann syndrome (BWS) is characterized by somatic
overgrowth and a predisposition to pediatric embryonal tumors. It is associated with genetic …

The concurrent development of cytogenetic, clinical, genetic and molecular studies has led
to the recognition that the different hereditary and non-hereditary forms of the Beckwith …

A recent series of observations has suggested a linkbetween in vitro fertilization (IVF) and
imprinting disorders, such as Beckwith-Wiedemann syndrome (BWS [MIM 130650]) and …

Beckwith–Wiedemann syndrome (BWS) is an imprinting disorder characterized by
overgrowth, tumor predisposition, and congenital malformations. Approximately 85% of …

Beckwith–Wiedemann syndrome (BWS) is a clinically heterogeneous overgrowth syndrome
associated with an increased risk for embryonal tumor development. BWS provides an ideal …

Beckwith–Wiedemann syndrome (BWS) is a congenital overgrowth condition with an
increased risk of developing embryonic tumours, such as Wilms' tumour. The cardinal …

Beckwith-Wiedemann syndrome (BWS) is a model imprinting disorder resulting from
mutations or epigenetic events involving imprinted genes at chromosome 11p15. 5. Thus …

Regional regulation of parental imprinting in the IGF2–H19 domain of imprinted genes was
studied in the Beckwith—Wiedemann syndrome (BWS). We identified BWS patients who …

Abstract Beckwith–Wiedemann Syndrome (BWS) results from mutations or epigenetic
events involving imprinted genes at 11p15. 5. Most BWS cases are sporadic and uniparental …