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Journal of Neurosurgery|March 10, 2001
Extent of tumor-brain interface: a new tool to predict evolution of malignant gliomasC A Valéry, B Marro, O Boyer, et al.Human Molecular Genetics|March 1, 1996
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisisM Konrad, S Saunier, L Heidet, et al.La Revue De Medecine Interne|June 7, 2005
[Immunohistochemistry contribution in Alport syndrome diagnosis]S Krichen Makni, M Kharrat, M Ben Hmida, et al.Endocrine|July 17, 1998
Regulation of amounts of mRNA for GnRH receptors by estradiol and progesterone in sheepB L Kirkpatrick, E Esquivel, P C Gentry, et al.The American Journal of Pathology|March 21, 1998
Somatic deletion of the 5' ends of both the COL4A5 and COL4A6 genes in a sporadic leiomyoma of the esophagusL Heidet, E Boye, Y Cai, et al.Kidney International|November 1, 1992
Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen geneC Antignac, J Zhou, M Sanak, et al.Kidney International|February 22, 2008
A missense mutation in podocin leads to early and severe renal disease in miceA Philippe, S Weber, E L Esquivel, et al.Genomics|July 15, 1994
Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneityM Medhioub, D Cherif, F Benessy, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 11, 1991
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkageJ S Beckmann, I Richard, D Hillaire, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 18, 2017
[Treatments of steroid-dependent nephrotic syndrome in children]A Couderc, E Bérard, V Guigonis, et al.Pageof 16