Meckel syndrome | Polycystic Kidney Disease: from Bench to Bedside
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
Characterizing the morbid genome of ciliopathies | Genome Biology | Full Text
Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report | BMC Medical Genetics | Full Text
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
TMEM67 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
TMEM67 Polyclonal Antibody | EpigenTek
MKS3 (NPHP11 or Meckelin or TMEM67) (Xenopus) antibody - BiCell Scientific®
TMEM67 Gene - GeneCards | MKS3 Protein | MKS3 Antibody
Joubert syndrome: congenital cerebellar ataxia with the molar tooth - The Lancet Neurology
TMEM67 Polyclonal Antibody (PA5-141155)
What is TMEM67 Gene Joubert syndrome type 6 NGS Genetic DNA Test ?
TMEM67, TMEM237, and Embigin in Complex With Monocarboxylate Transporter MCT1 Are Unique Components of the Photoreceptor Outer Segment Plasma Membrane - ScienceDirect
MKS3 (NPHP11 or Meckelin or TMEM67) antibody - BiCell Scientific®
Genes | Free Full-Text | Prenatal Versus Postnatal Diagnosis of Meckel–Gruber and Joubert Syndrome in Patients with TMEM67 Mutations
MKS3/TMEM67 mutations in patients with nephronophthisis (NPHP) and... | Download Scientific Diagram
TMEM67 Fusion Protein Ag5174 | Proteintech
TMEM67 Polyclonal Antibody (PA5-141155)
TMEM67 Antibody (ABIN2856740)
Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation | Scientific Reports
The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5 | Scientific Reports
JCI Insight - TRPV4 antagonists ameliorate ventriculomegaly in a rat model of hydrocephalus
Anti-TMEM67 Antibody Products | Biocompare
