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Craniofacial abnormality
Syndromic and Complex Craniosynostosis: Craniosynostosis: and Complex Syndromic
Letter to Editor Sep 2012; Vol 22 (No 3), Pp: 432-433
Brachycephaly and Syndactyly: Apert's Syndrome
Medically Necessary Orthodontic Treatment – Dental
Radial, Renal and Craniofacial Anomalies: Baller-Gerold Syndrome
Prenatal Ultrasonography of Craniofacial Abnormalities
Lingual Agenesis: a Case Report and Review of Literature
Three-Dimensional Ultrasound Study of Fetal Craniofacial Anatomy
Attenuation of Signaling Pathways Stimulated by Pathologically Activated FGF-Receptor 2 Mutants Prevents Craniosynostosis
Dissociated Eye Movements in Craniosynostosis: a Hypothesis Revived Br J Ophthalmol: First Published As 10.1136/Bjo.77.9.563 on 1 September 1993
Craniofacial Diseases Caused by Defects in Intracellular Trafficking
Letter to Editor Sep 2012; Vol 22 (No 3), Pp: 432-433
Inactivation of Sonic Hedgehog Signaling and Polydactyly in Limbs of Hereditary Multiple Malformation, a Novel Type of Talpid Mutant
AP-2-Null Cells Disrupt Morphogenesis of the Eye, Face, and Limbs in Chimeric Mice
Craniofacial Disorders Associated with Airway Obstruction in the Neonate
Identification of Apoptosis Pathway in Treacher Collins Syndrome Khaled Alsayegh Virginia Commonwealth University
7.1 Birth Defects Code List
Exome Sequencing Identifies Mutations in ANKRD11 in Two Patients with Cornelia De Lange-Overlappi
Top View
Mandibular Distraction Osteogenesis in the Management of Airway Obstruction in Children with Micrognathia: a Systematic Review
Increased Fgf and Hh Signaling Impairs Craniofacial and Limb
Analysis of 19 Own Cases and Review of the Literature
Capstone December
Psychosocial Development of Children with Treacher Collins Syndrome
AP-2-Null Cells Disrupt Morphogenesis of the Eye, Face, and Limbs in Chimeric Mice
The Neonate with Minor Dysmorphisms the Neonate with Minor Dysmorphisms
Congenital Malformations in River Buffalo (Bubalus Bubalis)
Recurrent Ptosis in a Case of Dubowitz Syndrome
Snrpb, the Gene Mutated in CCMS, Is Haploinsufficient and Required for Proper Morphogenesis and Splicing
The Application of Molecular Genetics to Detection of Craniofacial Abnormality