Pages that link to "De novo mutation"

Showing 50 items.

• Muscular dystrophy (links | edit)
• Huntington's disease (links | edit)
• Androgen insensitivity syndrome (links | edit)
• Rett syndrome (links | edit)
• Attention deficit hyperactivity disorder (links | edit)
• Ornithine decarboxylase (links | edit)
• Coding region (links | edit)
• Progeria (links | edit)
• De novo (links | edit)
• Kabuki syndrome (links | edit)
• Osteogenesis imperfecta (links | edit)
• Hallermann–Streiff syndrome (links | edit)
• Treacher Collins syndrome (links | edit)
• Germline mutation (links | edit)
• Cri du chat syndrome (links | edit)
• Coffin–Lowry syndrome (links | edit)
• Birt–Hogg–Dubé syndrome (links | edit)
• Torsion dystonia (links | edit)
• Lennox–Gastaut syndrome (links | edit)
• Facioscapulohumeral muscular dystrophy (links | edit)
• Inbreeding depression (links | edit)
• Histone H4 (links | edit)
• Otocephaly (links | edit)
• Causes of autism (links | edit)
• List of Latin phrases (full) (links | edit)
• Familial hemiplegic migraine (links | edit)
• X-linked severe combined immunodeficiency (links | edit)
• Spinal muscular atrophy (links | edit)
• 1p36 deletion syndrome (links | edit)
• Neurofibromin (links | edit)
• DNM (links | edit)
• Alternating hemiplegia of childhood (links | edit)
• Hemiplegic migraine (links | edit)
• Mendelian error (links | edit)
• Coffin–Siris syndrome (links | edit)
• GABRB3 (links | edit)
• SCN1A (links | edit)
• POLD1 (links | edit)
• KCNH1 (links | edit)
• CHD2 (links | edit)
• ISCU (links | edit)
• Intellectual disability (links | edit)
• 18p- (links | edit)
• ALS (links | edit)
• Metabolic myopathy (links | edit)
• Congenital hemolytic anemia (links | edit)
• Syringocystadenoma papilliferum (links | edit)
• List of Latin phrases (D) (links | edit)
• Neurogenomics (links | edit)
• Nicolaides–Baraitser syndrome (links | edit)