## Abstract Yunis–Varon syndrome (YVS) is a rare autosomal recessive condition characterized by limb defects, ossification defects, generalized hypotrichosis and, frequently, a severe neonatal course. The molecular basis is unknown. We report on a newborn infant with previously undescribed findings
Nicolaides–Baraitser syndrome: Delineation of the phenotype
✍ Scribed by Sérgio B. Sousa; Omar A. Abdul-Rahman; Armand Bottani; Valérie Cormier-Daire; Alan Fryer; Gabriele Gillessen-Kaesbach; Denise Horn; Dragana Josifova; Alma Kuechler; Melissa Lees; Kay MacDermot; Alex Magee; Fanny Morice-Picard; Elizabeth Rosser; Ajoy Sarkar; Nora Shannon; Irene Stolte-Dijkstra; Alain Verloes; Emma Wakeling; Louise Wilson; Raoul C.M. Hennekam
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 439 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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