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A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3
(American Journal Human Genetic ; 68 (1 p. 269-274, 2001)
Autosomal recessive Charcot-Marie-Tooth disease (CMT) represents a heterogeneous group of disorders affecting the peripheral nervous system. The axonal form of the disease is designated as "CMT type 2" (CMT2), and one locus ...
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3
(Neurimuscular Disorder 14 (5) 301-306, 2004)
Cbarcot-Marie-Tooth disease (CMT) comprises a heterogeneous group of hereditary motor and sensory peripheral neuropathies. The
autosomal recessive axonal form of CMT (ARCMT2) is ram. Eight patients of a large consanguineous ...
Análisis de varios marcadores genéticos clásicos en la población de Costa Rica
(2001)
A study of several loci blood groups (ABO, Diego, Duffy, Kell, Kidd, Lewis, Lutheran, MNSs, P,
Rhesus and Secretor), and Hp serum protein was carried out on a sample of 2 196 unrelated Costa Rican individuals
of both ...