Pages that link to "Q5034093"

The following pages link to Cantú syndrome (Q5034093):

Displaying 32 items.

• KCNJ8 (Q18028182) (← links)
• ABCC9 (Q18034993) (← links)
• (Q26492785) (redirect page) (← links)
• Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly). (Q34069985) (← links)
• Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations (Q34147616) (← links)
• Cantú syndrome resulting from activating mutation in the KCNJ8 gene (Q34778748) (← links)
• Cantú syndrome is caused by mutations in ABCC9. (Q36017136) (← links)
• Neurologic and neuroimaging manifestations of Cantú syndrome: A case series (Q37113389) (← links)
• Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition (Q37515507) (← links)
• Cantú Syndrome Associated with Ovarian Agenesis (Q44454472) (← links)
• Cantú syndrome with coexisting familial pituitary adenoma (Q48256123) (← links)
• A patient with Cantú syndrome associated with fatal bronchopulmonary dysplasia and pulmonary hypertension. (Q53287377) (← links)
• cantu sanchez-corona hernandez syndrome (Q55789835) (← links)
• Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders (Q57812209) (← links)
• Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype (Q58443353) (← links)
• Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome (Q58443467) (← links)
• Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings (Q73806939) (← links)
• Short-term follow-up of a Brazilian patient with Cantú syndrome (Q83782734) (← links)
• Cantú syndrome, the changing phenotype: a report of the two oldest Dutch patients (Q88212636) (← links)
• Three-dimensional facial morphology in Cantú syndrome (Q89888631) (← links)
• A new type of ATP-sensitive potassium channelopathy : Cantú syndrome (Q90232853) (← links)
• Novel variants of ABCC9 in Japanese children with Cantú syndrome (Q90556432) (← links)
• A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with Cantú syndrome (Q90677725) (← links)
• Cantú syndrome as a rare cause of pericardial effusion in a young woman (Q91850362) (← links)
• Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry (Q91908342) (← links)
• Glibenclamide treatment in a Cantú syndrome patient with a pathogenic ABCC9 gain-of-function variant: Initial experience (Q92598952) (← links)
• Cantú Syndrome and Related Disorders (Q95604664) (← links)
• Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants (Q97082539) (← links)
• Cantú syndrome with novel pathogenic variant in nucleotide-binding domain 1 of ABCC9 (Q99412610) (← links)
• The Mechanism of High-Output Cardiac Hypertrophy Arising From Potassium Channel Gain-of-Function in Cantú Syndrome (Q99632889) (← links)
• Wikidata:Database reports/Constraint violations/P486 (← links | edit)
• Wikidata:WikiCite/Wikidata lists/Usage of Scholia in Template Medical resources on the English Wikipedia (← links | edit)