congenital hepatic fibrosis) cause COACH syndrome (Joubert syndrome with ) RPGRIP1L and CC2D2A , MKS3 Mutations in 3 genes (
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Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center - Ophthalmology
congenital hepatic fibrosis) cause COACH syndrome (Joubert syndrome with ) RPGRIP1L and CC2D2A , MKS3 Mutations in 3 genes (
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Joubert syndrome in siblings: A rare case report with literature review Venkataramaiah VD, Patil AT, Sathyanarayana VH - Apollo Med
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i-year-old girl with COACH syndrome. A, Longitudinal sonogram through... | Download Scientific Diagram
![PDF] Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome | Semantic Scholar PDF] Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ecffa3e33a43f9668e87abd84c5a76746ac21797/2-Figure1-1.png)
PDF] Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome | Semantic Scholar
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Joubert syndrome: Clinical and radiological characteristics of nine patients Elhassanien AF, Alghaiaty HA - Ann Indian Acad Neurol
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