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Cancer Research|October 19, 2001
Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposisK Heinimann, A Thompson, A Locher, 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|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.La Revue De Medecine Interne|June 7, 2005
[Immunohistochemistry contribution in Alport syndrome diagnosis]S Krichen Makni, M Kharrat, M Ben Hmida, et al.Nephrologie|January 1, 1996
[Value of cyclosporine in the treatment of the recurrence of nephrosis after renal transplantation]B Ranchin, M F Gagnadoux, M Broyer, et al.Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.The American Journal of Pathology|February 10, 2000
Twin-to-twin transfusion syndrome. Role of the fetal renin-angiotensin systemD Mahieu-Caputo, M Dommergues, A L Delezoide, et al.Human Molecular Genetics|March 21, 1998
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisisS Saunier, J Calado, R Heilig, et al.Journal of the American Society of Nephrology : JASN|March 1, 1995
Structural-functional relationships in Alport syndromeK H Kim, Y Kim, M C Gubler, et al.Pageof 23