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Year | Number of Results |
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1996 | 1 |
1999 | 2 |
2001 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 356581
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Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins.
DNA Res. 2001 Dec 31;8(6):319-27. doi: 10.1093/dnares/8.6.319.
DNA Res. 2001.
PMID: 11853319
Free article.
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1.
Guilbot A, Ravisé N, Bouhouche A, Coullin P, Birouk N, Maisonobe T, Kuntzer T, Vial C, Grid D, Brice A, LeGuern E.
Guilbot A, et al.
Eur J Hum Genet. 1999 Dec;7(8):849-59. doi: 10.1038/sj.ejhg.5200382.
Eur J Hum Genet. 1999.
PMID: 10602360
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Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.
Gabreëls-Festen A, van Beersum S, Eshuis L, LeGuern E, Gabreëls F, van Engelen B, Mariman E.
Gabreëls-Festen A, et al.
J Neurol Neurosurg Psychiatry. 1999 May;66(5):569-74. doi: 10.1136/jnnp.66.5.569.
J Neurol Neurosurg Psychiatry. 1999.
PMID: 10209165
Free PMC article.
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Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.
LeGuern E, Guilbot A, Kessali M, Ravisé N, Tassin J, Maisonobe T, Grid D, Brice A.
LeGuern E, et al.
Hum Mol Genet. 1996 Oct;5(10):1685-8. doi: 10.1093/hmg/5.10.1685.
Hum Mol Genet. 1996.
PMID: 8894708
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