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Neuropediatrics|August 25, 2001
Respiratory chain deficiency in Alpers syndromeM Gauthier-Villars, P Landrieu, V Cormier-Daire, et al.
The Journal of Clinical Investigation|June 1, 1994
Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiencyT Bourgeron, D Chretien, J Poggi-Bach, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.
Human Mutation|April 27, 2004
Allelic heterogeneity of SMARD1 at the IGHMBP2 locusI Maystadt, M Zarhrate, P Landrieu, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
Journal of Neurosurgery|March 1, 1997
Subdural sarcoma associated with chronic subdural hematoma. Report of two cases and review of the literatureG Cinalli, M Zerah, M Carteret, et al.
The European Journal of Medicine|October 1, 1992
Non-Hodgkin's lymphoma associated with primary Sjögren's syndromeD Pariente, J M Anaya, B Combe, et al.
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