| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0028-3770(06)71216-4 |
| P698 | PubMed publication ID | 16981654 |
| P2093 | author name string | E Arnaud | |
| D Marchac | |||
| D Renier | |||
| P2860 | cites work | Craniosynostosis, midfacial hypoplasia, and foot abnormalities: An autosomal dominant phenotype in a large Amish kindred | Q28200922 |
| Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis | Q28266282 | ||
| Dominant erbliche Akrocephalosyndaktylie | Q29307343 | ||
| Multiple-birth infants at higher risk for development of deformational plagiocephaly. | Q33537207 | ||
| The differential diagnosis of posterior plagiocephaly: true lambdoid synostosis versus positional molding | Q34063319 | ||
| Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans | Q34289809 | ||
| Classification of previously unclassified cases of craniosynostosis | Q34414601 | ||
| Upper and lower airway compromise in the Apert syndrome | Q35804850 | ||
| Prognosis for mental function in Apert's syndrome | Q36805126 | ||
| Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome. | Q37062973 | ||
| ??? | Q56335768 | ||
| The central nervous system in the Apert syndrome | Q38140616 | ||
| Carpenter's syndrome: Acrocephalopolysyndactyly. An autosomal recessive syndrome | Q38540463 | ||
| Localization of craniosynostosis Adelaide type to 4p16. | Q39375446 | ||
| Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull | Q40421394 | ||
| Spinal Anomalies in Pfeiffer Syndrome | Q40441504 | ||
| Saethre-Chotzen syndrome | Q40691648 | ||
| Skeletal abnormalities in the Apert syndrome | Q40793423 | ||
| Visceral anomalies in the Apert syndrome | Q40888817 | ||
| Grave'S's disease, an unusual complication: raised intracranial pressure due to premature fusion of skull sutures | Q42169580 | ||
| Craniosynostosis and fetal exposure to sodium valproate | Q43795299 | ||
| Occipital plagiocephaly: a critical review of the literature | Q47330501 | ||
| Agenesis of the corpus callosum and limbic malformation in Apert syndrome (type I acrocephalosyndactyly). | Q48212624 | ||
| Clinical variability in patients with Apert's syndrome | Q48269617 | ||
| Management of hearing loss in Apert syndrome | Q50472590 | ||
| Cervical spine in the Apert syndrome. | Q51687011 | ||
| The concurrence of hydrocephalus and craniosynostosis. | Q54344387 | ||
| Tracheal anomalies in Pfeiffer syndrome | Q56343133 | ||
| Surgical management of the hand in Apert syndrome | Q56349570 | ||
| Syndactyly in Apert syndrome. Utility of a prognostic classification | Q56379686 | ||
| Unilateral lambdoid synostosis: morphological characteristics | Q56380302 | ||
| [Mental prognosis of Apert syndrome] | Q56383772 | ||
| Congenital cervical spinal fusion: a study in Apert syndrome | Q56383836 | ||
| Lambdoid synostosis is an overdiagnosed condition | Q56384154 | ||
| Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture | Q56384329 | ||
| Cutaneous manifestations of Apert syndrome | Q56384385 | ||
| Jackson-Weiss syndrome: clinical and radiological findings in a large kindred and exclusion of the gene from 7p21 and 5qter | Q56387206 | ||
| Newly recognized autosomal dominant disorder with craniosynostosis | Q56391868 | ||
| The Antley-Bixler syndrome | Q56417528 | ||
| Basic fibroblast growth factor and transforming growth factor beta-1 expression in the developing dura mater correlates with calvarial bone formation | Q73400716 | ||
| P433 | issue | 2-3 Pt 2 | |
| P921 | main subject | craniosynostosis | Q378183 |
| P304 | page(s) | 200-227 | |
| P577 | publication date | 2006-06-01 | |
| P1433 | published in | Neuro-chirurgie | Q26867030 |
| P1476 | title | [Classification of craniosynostosis] | |
| P478 | volume | 52 |
| Q50436689 | Intracranial and Extracranial Malformations in Patients With Craniofacial Anomalies | cites work | P2860 |
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