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Identification of a novel causative mutation in the ROR2 gene in a Lebanese family with a mild form of recessive Robinow syndrome

✍ Scribed by Cybel Mehawej; Eliane Chouery; Diane Maalouf; Geneviève Baujat; Martine Le Merrer; Valérie Cormier-Daire; André Mégarbané


Book ID
116433435
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
743 KB
Volume
55
Category
Article
ISSN
1769-7212

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