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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]D Graber, C Antignac, G Deschenes, et al.
Human Molecular Genetics|November 11, 1999
Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosinM Attard, G Jean, L Forestier, et al.
Neuropediatrics|August 1, 1988
Multiple sclerosis in children: report of clinical and paraclinical features of 19 casesB Boutin, E Esquivel, M Mayer, et al.
Pediatric Nephrology (Berlin, Germany)|October 31, 2001
Benign familial hematuria associated with a novel COL4A4 mutationS Ozen, D Ertoy, L Heidet, et al.
The International Journal of Pediatric Nephrology|January 1, 1985
Diffuse arterial calcified elastopathy--a new cause of renovascular hypertension in childrenM C Gubler, C Antignac, M Broyer, et al.
Genomics|July 1, 1990
Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumorC Jeanpierre, C Antignac, C Beroud, et al.
Biology of Reproduction|July 1, 1997
The estradiol-induced luteinizing hormone surge in the ewe is not associated with increased gonadotropin-releasing hormone messenger ribonucleic acid levelsH Dhillon, A M Dunn, E Esquivel, et al.
Surgical Oncology Clinics of North America|April 1, 1996
Gene therapy for liver tumorsY Panis, A R Rad, O Boyer, et al.
Kidney International. Supplement|July 1, 1993
A specific glomerular lesion of the graft: allograft glomerulopathyR Habib, A Zurowska, N Hinglais, et al.
Kidney International|April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distributionM C Gubler, B Knebelmann, A Beziau, et al.
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