Hereditary neuropathy with liability to pressure palsies: Two cases with a reciprocal translocation t(16;17)(q12;p11.2) interrupting the PMP22 gene

M. Nadal, A. Valiente, A. Domenech, M. Pritchard, Xavier P. Estivill, M. A. Ramos-Arroyo

Research output: Contribution to journalLetter

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)396-398
Number of pages3
JournalJournal of Medical Genetics
Volume37
Issue number5
Publication statusPublished - 2000
Externally publishedYes

Fingerprint

Hereditary Sensory and Motor Neuropathy
Myelin Proteins
Chromosomes, Human, Pair 16
Genetic Translocation
Chromosomes, Human, Pair 17
Cytogenetic Analysis
Pedigree
Genes
Tomaculous neuropathy

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Hereditary neuropathy with liability to pressure palsies : Two cases with a reciprocal translocation t(16;17)(q12;p11.2) interrupting the PMP22 gene. / Nadal, M.; Valiente, A.; Domenech, A.; Pritchard, M.; Estivill, Xavier P.; Ramos-Arroyo, M. A.

In: Journal of Medical Genetics, Vol. 37, No. 5, 2000, p. 396-398.

Research output: Contribution to journalLetter

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