A Case of <i>FAM111A</i>-Associated Kenny-Caffey Syndrome Type 2 with New Clinical Features: Microtia, Lacunar Skull Appearance, and Arnold-Chiari Malformation. [PDF]
Mol SyndromolDoğan Arı AB +4 more
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Liveborn trisomy 22: a case report. [PDF]
Front PediatrJares Baglivo S +4 more
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Outcomes of Bonebridge Implantation in 10 Patients with Rare Genetic Syndromes and Difficult Anatomy. [PDF]
J Clin MedCywka KB +3 more
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Vacuum-Assisted Closure Device as a Suction Tool in First Stage Autologous Auricular Reconstruction. [PDF]
J Maxillofac Oral SurgSawiris MA, Kamel I, Badawy MS.
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Molecular diagnosis of rare biallelic CDC45 gene variants causing Meier-Gorlin syndrome-7 using whole exome sequencing. [PDF]
Hum GenomicsZhuang J, Huang N, Wang J, Chen C.
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Innovative Approaches in Microtia Treatment: Advancements in Tissue Engineering and Scaffold Design. [PDF]
Ann Biomed EngNúñez JAV +5 more
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Novel 3D-printed aids for total ear reconstruction. [PDF]
3D Print MedSchoenfeld L +6 more
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Two-dimensional and three-dimensional ultrasonographic diagnosis of congenital auricular anomalies. [PDF]
Front Med (Lausanne)Wang H +9 more
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Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy. [PDF]
Orphanet J Rare DisLi C +7 more
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