Wiedemann-Rautenstrauch syndrome: A phenotype analysis

Author:

Paolacci Stefano1ORCID,Bertola Debora2ORCID,Franco José2,Mohammed Shehla3,Tartaglia Marco4,Wollnik Bernd5,Hennekam Raoul C.6

Affiliation:

1. Department of Experimental Medicine; “Sapienza” University of Rome; Rome Italy

2. Unidade de Genética do Instituto da Criança; Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo; São Paulo Brazil

3. Department of Clinical Genetics; Guy's Hospital; London United Kingdom

4. Genetics and Rare Diseases Research Division; Ospedale Pediatrico Bambino Gesù; Rome Italy

5. Institute of Human Genetics; University Medical Center Göttingen; Göttingen Germany

6. Department of Pediatrics; Academic Medical Center; University of Amsterdam; Amsterdam The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference86 articles.

1. A new case of neonatal progeroid syndrome with agenesis of corpus callosum;Abdel-Salam;Genetic Counseling,1999

2. A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2;Akawi;Birth Defects Research Part A Clinical and Molecular Teratology,2013

3. What syndrome is this? Wiedemann-Rautenstrauch syndrome;Almeida;Pediatric Dermatology,2005

4. Genetic heterogeneity in 26 infants with a hypomyelinating leukodystrophy;Arai-Ichinoi;Human Genetics,2016

5. Wiedemann-Rautenstrauch neonatal progeroid syndrome: Report of three new patients;Arboleda;Journal of Medical Genetics,1997

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