We describe three unrelated cases of Wiedemann‐Beckwith syndrome (WBS). Two of them
were diagnosed postnatally while the third was detected during pregnancy that resulted in …

We have studied a family in which four members of the same generation were affected with
Wiedemann‐Beckwith syndrome (WBS). Trisomy 11p15 was demonstrated using molecular …

Genomic imprinting of chromosome arm 11p is involved in the Wiedemann‐Beckwith
syndrome (WBS). About 20% of patients with sporadic WBS have paternal uniparental …

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome with variable
expression. The major features are anterior abdominal wall defects, macroglossia, and …

A baby with Wiedemann‐Beckwith syndrome (WBS) and her phenotypically normal mother
carried the same paracentric inversion, inv (11)(p11. 2 15.5), in the short arm of …

Beckwith–Wiedemann syndrome (BWS) is an overgrowth syndrome characterized by
macrosomia, macroglossia, omphalocele, hemihyperplasia, and increased tumor risk. BWS …

We conducted a follow‐up study on 15 patients with Wiedemann‐Beckwith syndrome (WBS)
to further clarify major and minor diagnostic clinical characteristics and long‐term …

A new family with Wiedeman-Beckwith Syndrome is reported. All the affected subjects are
conceived from normal sisters. In two cases, antenatal diagnosis has been established by …

Wiedemann‐Beckwith syndrome (WBS) may be associated with abdominal tumors,
including Wilms tumor, adrenocortical carcinoma, hepatoblastoma, gonadoblastoma …

We report on the prenatal diagnosis of Beckwith‐Wiedemann syndrome (BWS) in a
pregnancy monitored because of a previously affected child. The proposita had classical …