Category: Array-CGH

Charcot-Marie-Tooth Disease, Demyelinating, Type 1a; CMT1A – Analysis by Oligo Array

Hereditary Neuropathy, with liability to pressure palsies; HNPP – Oligo Array

Neuropathy Hereditary with Liability to Pressure Palsies HNPP (PMP22 – 17p12)

Kallmann Syndrome, KAL1 (delXp22.31)

Digeorge Syndrome (del22q11.2)

Angelman Syndrome (15q11.2-q13)

Charcot-Marie-Tooth Disease type 1A Demyelinating (PMP22 – dup17p12)

Wolf-Hirschhorn Syndrome (del4p16.3)

Sotos Syndrome (NSD1 – 5q35.2-q35.3)

Prader-Willi Syndrome (15q11.2)