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Jean-Pierre Kerckaert

university of lille

5

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352

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SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes†

2011 Human Mutation
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Thrombocytopenia-absent radius (TAR) syndrome: A clinical genetic series of 14 further cases. Impact of the associated 1q21.1 deletion on the genetic counselling

2011 European Journal of Medical Genetics
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Étude transcriptomique de cellules mononucléées sanguines de patients parkinsoniens porteurs de la mutation G2019S de LRRK2

2010 Revue Neurologique
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Genomic Regions Supporting microRNA Expression and Their Biogenesis Are Globally Conserved in Diffuse Large B-Cell Lymphomas (DLBCL) and Display a Limited Number of Homozygous Deletions or Amplifications.

2007 Blood
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LAZ3 rearrangements in non-Hodgkin's lymphoma: correlation with histology, immunophenotype, karyotype, and clinical outcome in 217 patients

1994 Blood
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