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Health & Medicine Medical tourism in Croatia: Stem cell therapies

Medical Tourism in Croatia - safe and affordable stem cell therapies. ME-DENt clinic. Breast augmentation using stem cells from fat tissue.

Documents Analisis Estetico Facial de Farkas

 Leslie Farkas nació el 18 de abril de 1915, en Rózsahegy, Hungría (hoy Eslovaquia). Se graduó de la escuela de medicina en 1941 y sirvió como médico militar en…

Documents Non Carious Lesions

Non - Carious Lesions Due to Tooth Surface Loss: To Restore or Not to Restore? Mabi L. Singh, DMD, MS; Gerard Kugel, DMD, MS, PhD; Athena Papas DMD, PhD; and Britta Magnuson…

Documents lockjaw encodes a zebrafish tfap2a required for early neural crest development

Introduction The vertebrate neural crest forms the pigmentation of the body, peripheral innervation, and much of the cartilage and bone of the skull. Disruption of neural

Documents Craniosynostosis

CraniosynostosisContents lists avai Article Hist Received M * Commu Neurosurg Columbus, E-mail a 0887-8994/$ http://dx.do abstract Craniosynostosis is the premature fusion

Documents Major craniofacial defects: case series and prenatal diagnosis at the Instituto Nacional de...

es i Revista de Investigación Clínica / Vol. 64, Núm. 5 / Septiembre-Octubre, 2012 / pp 420-428 Major craniofacial defects: case series and prenatal

Documents Management of Lambdoid Craniosynostosis: A Comprehensive and Systematic Review

Management of Lambdoid Craniosynostosis: A Comprehensive and Systematic ReviewTaylor Reardon e aKentucky College of Osteopathic Medicine, Pikeville, KY, USA; bDesert Regional

Documents Pediatric Craniofacial

Komansky_Craniofacial_mechrel.inddOur goal is to return patients back to normal activities as soon as possible. That’s why we use the most advanced surgical treatments,

Documents Extreme Manifestation of a Familial Case of Treacher Collins Syndrome in an Infant with Arhinia,...

Volume 3 Issue 8 August 2020 Extreme Manifestation of a Familial Case of Treacher Collins Syndrome in an Infant with Arhinia, Eyelid Colobomas and Single Kidney Srijan Singh*

Documents De novo mutations in SMCHD1 abrogate nasal development

RADAR Research Archive and Digital Asset Repository Gordon, C., et al. (2017) 'De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal