Pages that link to "Q42215601"

The following pages link to NRAS Mutations in Noonan Syndrome. (Q42215601):

Displaying 8 items.

• Mutation in NRAS in familial Noonan syndrome--case report and review of the literature (Q26783023) (← links)
• Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders (Q36246158) (← links)
• Recalculation of 23 mouse HDL QTL datasets improves accuracy and allows for better candidate gene analysis (Q36709654) (← links)
• 1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency. (Q37217301) (← links)
• Noonan syndrome - a new survey (Q37549407) (← links)
• Ras/MAPK syndromes and childhood hemato-oncological diseases (Q38068387) (← links)
• Genotype and phenotype spectrum of NRAS germline variants (Q40180317) (← links)
• Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate (Q91915366) (← links)