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The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3
Journal of Cranio-Maxillofacial Surgery, 06/17/09

Dostal A et al. - Orofacial abnormalities are characteristic features of 18q- syndrome patients and potential CP/L critical region could be assumed at 18q22.3 between markers D18S879 and D18S1141. In addition, gene deficient mouse models for Sall3 or Tshz1 genes, which are located at the 18q22.3 critical region, displayed palate abnormality phenotype.

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Cement Leakage in Percutaneous Vertebroplasty for Osteoporotic Compression Fractures With or Without Intravertebral Clefts
American Journal of Roentgenology, 11/06/09 Relevance Score: 91%

The prevalence of otological manifestations in children with cleft palate
Indian Journal of Otolaryngology and Head & Neck Surgery, 10/07/09 Relevance Score: 88%

Occurrence of Central Polydactyly, Syndactyly, and Cleft Hand in a Single Family: Report of Five Hands in Three Cases
The Journal of Hand Surgery, 11/12/09 Relevance Score: 87%

Correction of Secondary Cleft Lip Deformity: The Whistle Flap Procedure
Plastic and Reconstructive Surgery, 11/05/09 Relevance Score: 87%

Clinical Implication of the Olfactory Cleft in Patients With Chronic Rhinosinusitis and Olfactory Loss
Archives of Otolaryngology, 10/21/09 Relevance Score: 87%