Peripheral Neuropathy in Cardiofaciocutaneous Syndrome
- 30 April 2007
- journal article
- case report
- Published by Elsevier BV in Pediatric Neurology
- Vol. 36 (4), 250-252
- https://doi.org/10.1016/j.pediatrneurol.2006.12.004
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patientsAmerican Journal of Medical Genetics, 2003
- PTPN11 mutations are not responsible for the Cardiofaciocutaneous (CFC) syndromeEuropean Journal of Human Genetics, 2003
- Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndromeHuman Genetics, 2002
- CFC index for the diagnosis of cardiofaciocutaneous syndromeAmerican Journal of Medical Genetics, 2002
- Tomaculous neuropathy: A clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p<11.2Muscle & Nerve, 1996
- New multiple congenital anomalies/mental retardation syndrome with cardio‐facio‐cutaneous involvement—the CFC syndromeAmerican Journal of Medical Genetics, 1986