TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The Lancet Neurology
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
Treatment of hydrocephalic Tmem67 -/-rats with TRPV4 agonist... | Download Scientific Diagram
MKS3 antibody (13975-1-AP) | Proteintech
What is TMEM67 Gene Joubert syndrome type 6 NGS Genetic DNA Test ?
Identification of two missense mutations in TMEM67. (a) Sequence... | Download Scientific Diagram
Anti-TMEM67 Antibody Products | Biocompare
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
Functional validation of novel MKS3/TMEM67 mutations in COACH syndrome | Scientific Reports
MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
Differential expression analysis of the Tmem67 −/− post-natal... | Download Scientific Diagram
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
Orientation defects in stereociliary hair bundles with uncoupling from... | Download Scientific Diagram
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
Interpreting TMEM67 missense variants of uncertain significance (VUS) in an animal model | bioRxiv
TMEM67 Polyclonal Antibody (PA5-141155)
TMEM67 Polyclonal Antibody | EpigenTek
Meckelin (TMEM67) Antibody | Abbexa Ltd
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
TMEM67 Polyclonal Antibody (PA5-141155)
Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report | BMC Medical Genetics | Full Text
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
