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Tests > by Disorder > N

Nager syndrome

Facial Dysostosis Panel

Nemaline myopathy

Congenital Myopathy Panel
Neuromuscular Disorders Exome
Neuromuscular Disorders Panel

Neonatal diabetes

6q24 Methylation-Specific MLPA
Comprehensive Neonatal Diabetes Mutation Analysis
Monogenic Diabetes Panel
Neonatal Diabetes Panel
UPD6 testing

Neonatal diabetes and hypothyroidism

Hypothyroidism Panel

Nephronophthisis

Nephronophthisis Panel

Neurodegeneration with Brain Iron Accumulation

Neurodegeneration with Brain Iron Accumulation (NBIA) Panel

Neuronal Ceroid-Lipofuscinoses (NCLs)

Neuronal Ceroid-Lipofuscinoses Panel

Neutropenia

Severe Congenital Neutropenia Panel

Nicolaides-Baraitser syndrome

Cornelia de Lange and Related Disorders Panel

Non-syndromic forms of epilepsy

Early Infantile Epileptic Encephalopathy (EIEE) Panel
Epilepsy Exome
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Department of Human Genetics