Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: A new variant
- 30 September 1993
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 123 (3) , 431-434
- https://doi.org/10.1016/s0022-3476(05)81752-4
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyNature, 1992
- Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.Journal of Medical Genetics, 1992
- Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.Journal of Medical Genetics, 1992
- Hereditary motor and sensory neuropathies.Journal of Medical Genetics, 1991
- Auditory Function in Hereditary Motor and Sensory Neuropathy (Charcot-Marie-Tooth Disease)Acta Oto-Laryngologica, 1987
- X‐linked motor‐sensory neuropathy type‐II with deafness and mental retardation: A new disorderAmerican Journal of Medical Genetics, 1985
- Genetic linkage evidence for heterogeneity in Charcot‐Marie‐Tooth neuropathy (HMSN type I)Annals of Neurology, 1983
- Audiologic Findings in Charcot-Marie-Tooth DiseaseJAMA Otolaryngology–Head & Neck Surgery, 1982
- THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND IIBrain, 1980
- Abnormal auditory evoked potentials in hereditary motor‐sensory neuropathyAnnals of Neurology, 1979