Positional cloning of genes involved in the Beckwith‐Wiedemann syndrome, hemihypertrophy, and associated childhood tumors
M Mannens, M Alders, B Redeker… - … : The Official Journal …, 1996 - Wiley Online Library
Abstract The Beckwith‐Wiedemann syndrome (BWS) is an overgrowth malformation
syndrome that occurs with an incidence of 1: 13,700 births. There is a striking incidence of …
syndrome that occurs with an incidence of 1: 13,700 births. There is a striking incidence of …
Analysis of gene dosage on chromosome 11 in children suffering from Beckwith-Wiedemann syndrome
PN Schofield, S Lindham, W Engström - European journal of pediatrics, 1989 - Springer
Abstract The Beckwith-Wiedemann syndrome (BWS) is composed of multiple congenital
malformations coupled with a high concurrent risk for the development of specific rare …
malformations coupled with a high concurrent risk for the development of specific rare …
Molecular biology of Beckwith‐Wiedemann syndrome
R Weksberg, JA Squire - … Oncology: The Official Journal of SIOP …, 1996 - Wiley Online Library
Beckwith‐Wiedemann syndrome (BWS) is an overgrowth syndrome associated with a
predisposition to embryonal tumors, most commonly Wilms'(WT). Overlapping clinical …
predisposition to embryonal tumors, most commonly Wilms'(WT). Overlapping clinical …
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
D Catchpoole, WW Lam, D Valler, IK Temple… - Journal of medical …, 1997 - jmg.bmj.com
Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome associated
with a characteristic pattern of visceromegaly and predisposition to childhood tumours. BWS …
with a characteristic pattern of visceromegaly and predisposition to childhood tumours. BWS …
11p15. 5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis
A Puech, L Ahnine, HJ Lüdecke, G Senger, A Ivens… - Genomics, 1992 - Elsevier
Constitutional and somatic chromosomal abnormalities of the chromosome 11p15 region
are involved in an overgrowth malformation syndrome, the Beckwith-Wiedemann syndrome …
are involved in an overgrowth malformation syndrome, the Beckwith-Wiedemann syndrome …
Allelic methylation of H19 and IGF2 in the Beckwith—Wiedemann syndrome
W Reik, K W. Brown, R E. Slatter, P Sartor… - Human molecular …, 1994 - academic.oup.com
Abstract Beckwith-Wiedemann syndrome (BWS) Is a congenital overgrowth syndrome with
associated embryonal tumours. Most BWS cases are sporadic but familial cases occur In …
associated embryonal tumours. Most BWS cases are sporadic but familial cases occur In …
Molecular genetics of Wiedemann‐Beckwith syndrome
Wiedemann‐Beckwith syndrome (WBS) is a heterogeneous overgrowth syndrome
associated with malformations and an elevated risk of developing embryonal tumors. WBS is …
associated with malformations and an elevated risk of developing embryonal tumors. WBS is …
Beckwith–wiedemann syndrome
R Weksberg, C Shuman… - American Journal of …, 2005 - Wiley Online Library
Beckwith–Wiedemann syndrome (BWS) is a clinically heterogeneous overgrowth syndrome
associated with an increased risk for embryonal tumor development. BWS provides an ideal …
associated with an increased risk for embryonal tumor development. BWS provides an ideal …
Molecular genetics of Beckwith-Wiedemann syndrome
Beckwith-Wiedemann syndrome (BWS) is an overgrowth disorder characterized by
developmental anomalies, tissue and organ hyperplasia, and an increased risk of …
developmental anomalies, tissue and organ hyperplasia, and an increased risk of …
Molecular basis of Beckwith–Wiedemann syndrome spectrum with associated tumors and consequences for clinical practice
Simple Summary Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn
overgrowth disorder caused by molecular alterations in chromosome 11p15. 5. These …
overgrowth disorder caused by molecular alterations in chromosome 11p15. 5. These …