Pages that link to "Q51935999"

The following pages link to Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations (Q51935999):

Displaying 21 items.

• Noonan syndrome (Q27001641) (← links)
• Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease (Q28259472) (← links)
• Noonan syndrome: clinical aspects and molecular pathogenesis (Q33806161) (← links)
• Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms (Q34440570) (← links)
• Noonan syndrome and clinically related disorders (Q34678373) (← links)
• A lethal course of hypertrophic cardiomyopathy in Noonan syndrome due to a novel germline mutation in the KRAS gene: case study (Q37487343) (← links)
• Hydrocephalus and Chiari type I malformation. (Q37934662) (← links)
• Diagnostically relevant facial gestalt information from ordinary photos (Q41014879) (← links)
• Genetics of congenital heart disease (Q41451951) (← links)
• Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling (Q47552779) (← links)
• Characterization of a novel KRAS mutation identified in Noonan syndrome (Q52162283) (← links)
• Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature. (Q52992343) (← links)
• An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences. (Q53711959) (← links)
• Clinical, pathological, and molecular analyses of cardiovascular abnormalities in Costello syndrome: a Ras/MAPK pathway syndrome. (Q54610891) (← links)
• Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotype. (Q54998566) (← links)
• Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: clinical evidence of crosslink between FGFR and RAS signaling pathways (Q56266841) (← links)
• KRAS gene mutations in Noonan syndrome familial cases cluster in the vicinity of the switch II region of the G-domain: report of another family with metopic craniosynostosis (Q56321587) (← links)
• Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation: a causal relationship? (Q57234950) (← links)
• Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case report (Q64044350) (← links)
• RASopathy in Patients With Isolated Sagittal Synostosis. (Q64910470) (← links)
• Age-Dependent De Novo Mutations During Spermatogenesis and Their Consequences (Q91844294) (← links)