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Clinical and Experimental Rheumatology|August 21, 2001
The Swiss German and Swiss French versions of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ)M Hofer, N Ruperto, R Saurenmann, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1R Dufourcq-Lagelouse, N Lambert, M Duval, et al.
Annales De Dermatologie Et De Venereologie|July 28, 1999
[Bi-symptomatic CINCA syndrome with inaugural urticaria and major articular lesions]G Guillet, D Dupré, M H Guillet, et al.
Human Genetics|August 14, 2001
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardationM Rio, C Ozilou, V Cormier-Daire, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
American Journal of Medical Genetics|December 26, 2001
Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literatureA Mégarbané, P Gosset, N Souraty, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Molecular mapping of twenty-four features of Down syndrome on chromosome 21J M Delabar, D Theophile, Z Rahmani, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Mapping of the Down syndrome phenotype on chromosome 21 at the molecular levelP M Sinet, D Théophile, Z Rahmani, et al.
Neuroscience Letters|November 25, 1991
Reduced protein kinase C activity in sporadic Alzheimer's disease fibroblastsA Bruel, G Cherqui, S Columelli, et al.
European Cytokine Network|June 5, 1998
Inflammation: "a natural experiment" for the systemic pathogenicity of cytokinesC Herbelin, P Roux-Lombard, A Herbelin, et al.
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