| Body na spoluautora | Body za publikaci pro MU | Odkaz ISVaV | | 0,56 | 2,25 | Substituce v promotoru CYP21 genu ovlivňující fenotyp nemoci u pacientů s deficitem 21-hydroxylázy
|
| 3,46 | 6,92 | Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease
|
| 0,00 | 0,00 | Experiences with mutation analysis of epidermolysis bullosa in the Czech republic
|
| 3,36 | 6,72 | ADVANCE IN MOLECULAR DIAGNOSIS OF FAMILIAL HYPECHOLESTEROLEMIA IN THE CZECH POPULATION: IDENTIFICATION AND CHARACTERIZATION OF LARGE REARRANGEMENTS IN LDLR GENE
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| 0,00 | 0,00 | Advance in molecular diagnosis of familial hypercholesterolemia in the Czech population: identification and characterization of large rearrangements in LDLR gene
|
| 0,00 | 0,00 | Advance in molecular diagnosis of familial hypercholesterolemia in the Czech population: identification and characterization of large rearrangements in LDLR gene
|
| 4,06 | 20,32 | Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy
|
| 11,00 | 11,00 | Molecular screening of Smith-Lemli-Opitz syndrome in pregnant women from the Czech Republic.
|
| 0,94 | 1,87 | Možnosti využití DNA čipů v molekulární diagnostice dědičných onemocnění
|
| 9,36 | 9,36 | Syndrom fragílního X chromozomu typu FRAXE: klinická a molekulárně-genetická diagnostika
|
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(c) Michal Bulant, 2011