Received in revised version 24 November 1995, accepted for publication 3 May 1996 and
Martinez y Martinez et al.), as well as to show the frequencies of features analyzed in one or …

We describe 18 individuals from five unrelated families with various manifestations of the
Wiedemann‐Beckwith syndrome. Pedigree analysis was performed on the 5 families and on …

A pair of monozygotic twins discordant for Wiedemann-Beckwith syndrome is described. The
probability of monozygosity is 0.995. This observation suggests that the syndrome is unlikely …

Wiedemann‐Beckwith syndrome (WBS) has attracted a great deal of attention because of its
genetic complexity. Individuals with WBS can be identified objectively by anthropometric …

We report 3 pairs of monozygotic (MZ) twins, one twin showing typical Wiedemann‐Beckwith
syndrome (WBS) with minimal or no expression of the condition in the co‐twin. These cases …

We report four additional cases of Wiedemann‐Beckwith syndrome (WBS): A mother, her
brother, and two of her children (half‐sibs). Theories of the genetic transmission of the WBS …

OBJECTIVE: Wiedemann-Beckwith syndrome is a multisystemic pattern of congenital
anomalies with overgrowth. The most characteristic clinical features are macroglossia, high …

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 …

We have carried out a follow‐up study of 13 children with Wiedemann‐Beckwith syndrome
(WBS) using a standard protocol which included facial anthropometric measurements. We …

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 …