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Syndromic Craniosynostosis
Institution:1. Department of Otolaryngology---Head and Neck Surgery, Texas Tech University Health Sciences Center, 3601 4th Street, Stop 8312, Lubbock, TX 79430, USA;2. Department of Otolaryngology---Head and Neck Surgery, University of Cincinnati, Cincinnati, OH, USA;3. Pediatric Neurosurgery, Department of Pediatrics, West Texas Craniofacial Center of Excellence, Texas Tech University Health Sciences Center, 3601 4th Street, Lubbock, TX 79430, USA;4. Division of Facial Plastic and Reconstructive Surgery, Department of Otolaryngology---Head and Neck Surgery, West Texas Craniofacial Center of Excellence, Texas Tech University Health Sciences Center, 3601 4th Street, Stop 8312, Lubbock, TX 79430, USA;1. Children’s ENT and Facial Plastic Surgery, Children’s Hospitals and Clinics of Minnesota, 2530 Chicago Avenue South, Suite 450, Minneapolis, MN 55404, USA;2. Department of Otolaryngology, University of Minnesota, 420 Delaware Street Southeast, MMC 396, Minneapolis, MN 55455, USA;3. Division of Pediatric Otolaryngology, University of Michigan CW5702, 1540 E. Hospital Drive, Ann Arbor, MI 48109, USA;1. Department of Plastic and Reconstructive Surgery and Hand Surgery, Craniofacial Center The Netherlands, Erasmus Medical Center Sophia Children''s Hospital, Rotterdam, The Netherlands;2. Department of Radiology, Craniofacial Center The Netherlands, Erasmus Medical Center Sophia Children''s Hospital, Rotterdam, The Netherlands;3. Department of Neurosurgery, Craniofacial Center The Netherlands, Erasmus Medical Center Sophia Children''s Hospital, Rotterdam, The Netherlands;4. Department of Pediatrics, Craniofacial Center The Netherlands, Erasmus Medical Center Sophia Children''s Hospital, Rotterdam, The Netherlands;5. Department of Neurosurgery, Great Ormond Street Hospital for Children, London, England, UK;1. Inserm 1033, neurochirurgie pédiatrique, centre de référence pour les craniosténoses, Lyon et université Claude Bernard Lyon 1, hôpital femme-mère-enfant, 69003 Lyon, France;2. Endocrinologie et diabète de l’enfant, filière OSCAR et plateforme d’expertise Paris Sud maladies rares, centre de référence des maladies rares du calcium et du phosphate, hôpital Bicêtre Paris Sud, AP–HP, 94270 Le Kremlin Bicêtre, France;3. Centre de référence maladies osseuses constitutionnelles, institut imagine, 75015 Paris, France;4. Inserm 1033, centre de référence des maladies rares du calcium et du phosphate, université Claude Bernard Lyon 1, hôpital femme-mère-enfant, 69003 Lyon, France;5. Service de radiologie pédiatrique, université Paris-Saclay, hôpital Bicêtre, AP–HP, 94270 Le Kremlin Bicêtre, France;6. GENDEV Team, CNRS UMR5292, CRNL, UCBL1, Inserm U1028, service de génétique, centre de référence anomalies du développement, centre de compétence maladies osseuses constitutionnelles, hospices civils de Lyon, 69003 Lyon, France;7. Inserm U1185, université Paris Sud Paris-Saclay, 94270 Le Kremlin Bicêtre, France
Abstract:
Keywords:Apert syndrome  Craniofacial syndromes  Crouzon syndrome  FGFR mutations  Muenke syndrome  Pfeiffer syndrome  Saethre-Chotzen syndrome  Syndromic craniosynostosis
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