Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: A reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients

✍ Scribed by Emilia Bellone; Angelo Schenone; Gianluigi Mancardi; Garth A Nicholson; Michele Abbruzzese; Franco Ajmar; Paola Mandich

• Book ID: 116125826
• Publisher: Elsevier Science
• Year: 1996
• Tongue: English
• Weight: 484 KB
• Volume: 213
• Category: Article
• ISSN: 0304-3940
• DOI: 10.1016/0304-3940(96)12825-1