New indirect method for estimating the birth prevalence of the Apert syndrome

Author:

Cohen M. Michael,Kreiborg Sven

Publisher

Elsevier BV

Subject

Otorhinolaryngology,Oral Surgery,Surgery

Reference17 articles.

1. Acquaviva R, Tamic PM, Lebascle J, Kerdoudi H, Berrada A. Les craniosténoses en milieu marocain. A propos de 140 observations. Neurochirurgie 12: 561-6.

2. The premature synostosis of the cranial sutures;Bertelsen;Acta Ophthalmol,1958

3. Apert's syndrome (a type of acrocephalosyndactyly) — observations on a British series of thirty-nine cases;Blank;Ann Hum Genet (Lond),1960

4. Craniosynostosis: diagnosis, evaluation, and management;Cohen,1986

5. Cohen MM Jr, Kreiborg S, Lammer EJ, et al. Birth prevalence study of the Apert syndrome. Am J Med Genet (in press).

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2. Apert's syndrome: A rare craniofacial disorder;Journal of Indian Society of Pedodontics and Preventive Dentistry;2020

3. Apert syndrome with congenital diaphragmatic hernia: another case report and review of the literature;Clinical Dysmorphology;2019-04

4. Surgical Correction of the Apert Craniofacial Deformities;Craniomaxillofacial Reconstructive and Corrective Bone Surgery;2019

5. Identification and Management of Cranial Anomalies in Perinatology;Clinics in Perinatology;2018-12

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