Table II from Joubert syndrome: long-term follow-up. | Semantic Scholar
![PDF] Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/2ce48d3340ab6814ea6312ed4609d79a59b20b36/4-Table1-1.png "PDF] Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome | Semantic Scholar")
PDF] Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome | Semantic Scholar
Joubert Syndrome 20 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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Figure 1 from Unraveling the genetics of Joubert and Meckel-Gruber syndromes. | Semantic Scholar
Manifestations of Cerebello-Oculo-Renal Syndromes | Download Table
congenital hepatic fibrosis) cause COACH syndrome (Joubert syndrome with ) RPGRIP1L and CC2D2A , MKS3 Mutations in 3 genes (
Joubert syndrome: Clinical and radiological characteristics of nine patients Elhassanien AF, Alghaiaty HA - Ann Indian Acad Neurol
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i-year-old girl with COACH syndrome. A, Longitudinal sonogram through... | Download Scientific Diagram
Joubert Syndrome 1 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Imaging findings in COACH syndrome.
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COACH syndrome associated with multifocal liver tumors | Semantic Scholar
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COACH syndrome associated with multifocal liver tumors | Semantic Scholar
Seven different MKS3/TMEM67 mutations in four families with... | Download Table
Mutation spectrum of Joubert syndrome and related disorders among Arabs | Human Genome Variation
Joubert syndrome in siblings: A rare case report with literature review Venkataramaiah VD, Patil AT, Sathyanarayana VH - Apollo Med
Coach Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Seven different MKS3/TMEM67 mutations in four families with... | Download Table
congenital hepatic fibrosis) cause COACH syndrome (Joubert syndrome with ) RPGRIP1L and CC2D2A , MKS3 Mutations in 3 genes (
![Figure 2. [Clinical features in JSRD]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK1325/bin/joubert-Image002.jpg "Figure 2. [Clinical features in JSRD]. - GeneReviews® - NCBI Bookshelf")