Strmecki, Lana
Lana Strmecki
VIAF ID: 2485154441729935460002 (Personal)
Permalink: http://viaf.org/viaf/2485154441729935460002
Preferred Forms
-
100 0 _ ‡a Lana Strmecki
-
100 1 _ ‡a Strmecki, Lana
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
---|---|
Determination of informativity for the intragenic polymorphic marker Bcl I and prenatal diagnosis of hemophilia A in Slovenian population |
![]() |
Developmental decisions in Dictyostelium discoideum : review |
![]() |
Določanje informativnosti za intragenski označevalec polimorfizma Bcl I in prenatalna diagnostika hemofilije pri slovenski populaciji |
![]() |
Genetika avtosomnodominantne policistične bolezni ledvic |
![]() |
Genotipizacija bolnikov s hemofilijo A v Sloveniji |
![]() |
Haemophilia A and Mucopolysaccharidosis I-H (Hurler Syndrome) : a case report |
![]() |
A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype |
![]() |
Inversions of the factor VIII gene in Slovenian patients with severe haemophilia A. |
![]() ![]() |
Iskanje in opredelitev mutacij gena za koagulacijski faktor VIII pri hemofiliji A : doktorska disertacija = Detection and characterization of coagulation factor VIII gene mutations in haemophilia A |
![]() |
Linkage of Slovenian ADPKD families to PKD1 locus |
![]() |
Looking for genes encoding steroid 11beta-hydroxylase in the fungus Cochliobolus lunatus |
![]() |
Molekularno genetska analiza in diagnostika hemofilije A v slovenski populaciji = Molecular genetic analysis and diagnosis of hemophilia A in slovenian population : magistrsko delo |
![]() |
Mutation analysis of the entire PKD1 gene: genetic and diagnostic implications |
![]() ![]() |
Mutational analysis of 30 Slovenian cystic fibrosis patients compared to known Slovenian and European CF mutation spectra |
![]() |
New polymorphism in intron 20 of CFTR gene |
![]() |
A novel mutation Q602STOP in exon 12 of the FVIII gene |
![]() ![]() |
De novo mutation in DMD gene in a patient with combined hemophilia A and Duchenne muscular dystrophy |
![]() ![]() |
PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease |
![]() ![]() |
The Position of the Polycystic Kidney Disease 1 (PKD1) Gene Mutation Correlates with the Severity of Renal Disease |
![]() ![]() |
A positively charged channel within the Smc1/Smc3 hinge required for sister chromatid cohesion |
![]() |
Priprava DNA-sond za Southernovo analizo delecij gena pri Duchenne/Beckerjevi mišični distrofiji : diplomsko delo |
![]() |
Proteomic and microarray analyses of the Dictyostelium Zak1-GSK-3 signaling pathway reveal a role in early development |
![]() |
Releasing Activity Disengages Cohesin's Smc3/Scc1 Interface in a Process Blocked by Acetylation. |
![]() |
Screen of 55 Slovenian haemophilia A patients: identification of 2 novel mutations (S-1R and IVS23+1G->A) and discussion of mutation spectrum |
![]() |
Screening for mutations in the factor VIII gene using the restriction enzyme TaqI |
![]() |
Summary of new CF mutations and DNA sequence polymorphisms 4005+121delTT deletion of intron mutation? |
![]() |