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Jedrzejowska H
Jedrzejowska H
Polish Academy of Sciences
Medicine
Pathology
Gene
Genetics
Surgery
8
Papers
21
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Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report.
2003
European Journal of Neurology
Andrzej Kochański
Hanna Drac
Jedrzejowska H
Irena Hausmanowa-Petrusewicz
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Citations (12)
[Charcot-Marie Tooth type X (CMTX) disease: clinical and genetic characteristics of eleven patients].
2002
Neurologia I Neurochirurgia Polska
Andrzej Kochański
Barbara Ryniewicz
Jedrzejowska H
Kabzińska D
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[The role of molecular genetics in diagnosis of hereditary motor-sensory neuropathy].
2000
Neurologia I Neurochirurgia Polska
Andrzej Kochański
Jedrzejowska H
Barbara Ryniewicz
Budny B
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[Genotype-phenotype correlation in hereditary motor-sensory neuropathy type IA associated with duplication in chromosome 17p11.2-12].
2000
Neurologia I Neurochirurgia Polska
Barbara Ryniewicz
Jedrzejowska H
Andrzej Kochański
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Mutation Screening of Charcot‐Marie‐Tooth Patients in Poland
1999
Annals of the New York Academy of Sciences
A. Kochański
Vincent Timmerman
Jedrzejowska H
Barbara Ryniewicz
A. Löfgren
E. De Vriendt
C. Van Broeckhoven
A. Latos-Bieleńska
I. Hausmanowa-Petrusewicz
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