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Early ultrasound diagnosis enabled appropriate genetic counselling to be given; neonatal complications, such as hypoglycaemic episodes, were prevented.<\/jats:p>","DOI":"10.1002\/pd.1970110306","type":"journal-article","created":{"date-parts":[[2007,3,4]],"date-time":"2007-03-04T05:34:34Z","timestamp":1172986474000},"page":"167-175","source":"Crossref","is-referenced-by-count":23,"title":["Prenatal diagnosis in autosomal dominant Beckwith\u2010Wiedemann syndrome"],"prefix":"10.1002","volume":"11","author":[{"given":"D. L.","family":"Viljoen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Z.","family":"Jaquire","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D. 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