COACH syndrome - Wikipedia
congenital hepatic fibrosis) cause COACH syndrome (Joubert syndrome with ) RPGRIP1L and CC2D2A , MKS3 Mutations in 3 genes (
The 'impostor' coach syndrome
![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")
Figure 2. [Clinical features in JSRD]. - GeneReviews® - NCBI Bookshelf
COACH syndrome Report of two brothers with congenital hepatic fibrosis cerebellar vermis hypoplasia oligophrenia ataxia and mental retardation
i-year-old girl with COACH syndrome. A, Longitudinal sonogram through... | Download Scientific Diagram
Figure 2 from Coach syndrome: the first case from Turkey. | Semantic Scholar
Mutation spectrum of Joubert syndrome and related disorders among Arabs | Human Genome Variation
Seven different MKS3/TMEM67 mutations in four families with... | Download Table
Joubert Syndrome 1 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Comparison of clinical features reported in COACH patients: our cohort... | Download Table
congenital hepatic fibrosis) cause COACH syndrome (Joubert syndrome with ) RPGRIP1L and CC2D2A , MKS3 Mutations in 3 genes (
COACH Syndrome
Table II from Joubert syndrome: long-term follow-up. | Semantic Scholar
Coach Syndrome disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Joubert Syndrome 20 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
PDF) Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome
![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
The molar tooth sign | Neurology
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
Joubert syndrome in siblings: A rare case report with literature review Venkataramaiah VD, Patil AT, Sathyanarayana VH - Apollo Med
Human malformations of the midbrain and hindbrain: review and proposed classification scheme - ScienceDirect
