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Hereditary neuropathy with liability to pressure palsies: two cases with a reciprocal translocation t(16;17)(q12;11.2) interrupting the PMP22 gene

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Bibliographic Details
Published in:	Journal of medical genetics 2000-05, Vol.37 (5), p.396-398
Main Authors:	Nadal, M, Valiente, A, Domènech, A, Pritchard, M, Estivill, X, Ramos-Arroyo, M A
Format:	Article
Language:	English
Subjects:	Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 17 Cytogenetic Analysis Female Hereditary Sensory and Motor Neuropathy - genetics Humans In Situ Hybridization, Fluorescence Letters to the Editor Male Myelin Proteins - genetics Pedigree Translocation, Genetic
Citations:	Items that cite this one
Online Access:	Get full text
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