Wiedemann-Beckwith syndrome: Autosomal-dominant inheritance in a family

Author:

Best Lyle G.,Hoekstra Ronald E.,Opitz John M.

Publisher

Wiley

Subject

Genetics(clinical)

Reference31 articles.

1. : Extreme cytomegaly of the adrenal fetal cortex, omphalocele, hyperplasia of kidneys and pancreas, and Leydig-cell hyperplasia. Another syndrome? Presented at Annual Meeting of Western Society for Pediatric Research, Los Angeles, California, Nov. 11, 1963.

2. : Hyperplastic fetal visceromegaly with macroglossia, omphalocele, cytomegaly of adrenal fetal cortex, postnatal somatic gigantism, and other abnormalities: Newly recognized syndrome. Proceedings of the American Pediatric Society, Seattle, Washington, June 16-18, 1964 (Abstr. 41).

3. THE BECKWITH-WIEDEMANN SYNDROME

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1. Expanded phenotype and cancer risk in patients with Beckwith–Wiedemann spectrum caused by CDKN1C variants;American Journal of Medical Genetics Part A;2024-06

2. Familial Beckwith‐Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping;American Journal of Medical Genetics Part A;2022-11-02

3. Macrodactyly;Congenital Anomalies of the Upper Extremity;2021

4. Macrodactyly;Congenital Anomalies of the Upper Extremity;2014-08-14

5. Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance;Hormone Research in Paediatrics;2013

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