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- [2] EXCLUSION ANALYSIS OF CHARCOT-MARIE-TOOTH NEUROPATHY (CMT1) WITH CHROMOSOME-1P MARKERS CYTOGENETICS AND CELL GENETICS, 1989, 50 (2-3): : 178 - 180
- [3] CHARCOT-MARIE-TOOTH TYPE I DISEASE (CMT-1) AFRICAN JOURNAL OF NEUROLOGICAL SCIENCES, 2015, 34 (01): : 72 - 84
- [7] NEPHROPATHY ASSOCIATED WITH CHARCOT-MARIE-TOOTH (CMT) DISEASE INTERNATIONAL JOURNAL OF PEDIATRIC NEPHROLOGY, 1985, 6 (03): : 232 - 232
- [8] POSSIBLE HETEROGENEITY IN THE LINKAGE BETWEEN AUTOSOMAL DOMINANT CMT1 (CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1) AND FY CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 688 - 689
- [10] LINKAGE BETWEEN AUTOSOMAL DOMINANT CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-1 (CMT1) AND HUMAN GLUCOCEREBROSIDASE (GBA) CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4): : 633 - 633