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Journal of Diabetes and Its Complications|March 19, 2021
Non-linear renal function decline is frequent in patients with type 2 diabetes who progress fast to end-stage renal disease and is associated with African-Caribbean ethnicity and HbA<sub>1c</sub> variabilityStanimir I Stoilov, Nikolaos Fountoulakis, Angeliki Panagiotou, et al.Journal of Medical Genetics|May 5, 1999
Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucomaM Plásilová, I Stoilov, M Sarfarazi, et al.Human Molecular Genetics|July 1, 1996
Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated familiesA N Akarsu, I Stoilov, E Yilmaz, et al.Nature Genetics|March 1, 1994
The gene for achondroplasia maps to the telomeric region of chromosome 4pM Velinov, S A Slaugenhaupt, I Stoilov, et al.American Journal of Human Genetics|April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1I Stoilov, A N Akarsu, I Alozie, et al.Pageof 2