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  European Molecular Genetics Quality Network (EMQN)

  EMQN 01-AMYL-26 Hereditary Amyloidosis

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  EMQN 01-AZF-26 Y-Chromosome Microdeletion Testing (AZF)

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  EMQN 01-BWS-26 Beckwith-Wiedemann and Silver-Russell syndromes (BWS/SRS)

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  EMQN 01-CAH-26 Congenital Adrenal Hyperplasia (CAH)

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  EMQN 01-CARD-26 Cardiac Disorders

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  EMQN 01-CF-26 Cystic Fibrosis (CF)

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  EMQN 01-CMT-26 Charcot-Marie-Tooth disease / Hereditary Neuropathy with liability for Pressure Palsies (CMT/HNPP)

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  European Molecular Genetics Quality Network (EMQN)

  EMQN 01-DM-26 Myotonic dystrophy (DM) (Types 1 and/or 2)

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  EMQN 01-FAP-MAP-26 Polyposis Syndromes (FAP, MAP)

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  EMQN 01-FH-26 Familial Autosomal Dominant Hypercholesterolemia (FH)

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  European Molecular Genetics Quality Network (EMQN)

  EMQN 01-FRAX-26 Fragile X Syndrome (FRAX)

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  European Molecular Genetics Quality Network (EMQN)

  EMQN 01-FRDA-26 Friedreich Ataxia (FRDA)

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