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[Analysis of specific sequences in female patients with Turner syndrome--initial study]. [electronic resource] by
- Vodicka, R
- Vrtĕl, R
- Adamová, K
- Zapletalová, J
- Lebl, J
- Santavý, J
- Santavá, A
- Kolárová, J
- Konvalinka, D
- Krejciríková, E
Producer: 20021001
In:
Casopis lekaru ceskych vol. 141
Availability: No items available.
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17.
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[Analysis of free foetal DNA in maternal plasma using STR loci]. [electronic resource] by
- Vodicka, R
- Vrtel, R
- Procházka, M
- Santavá, A
- Dusek, L
- Vrbická, D
- Singh, R
- Krejciríková, E
- Schneiderová, E
- Santavý, J
Producer: 20060411
In:
Casopis lekaru ceskych vol. 145
Availability: No items available.
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18.
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[RHD genotyping from cell-free fetal DNA circulating in pregnant women peripheral blood and sensitivity assessment of innovated diagnostic approaches for introduction into the clinical practice]. [electronic resource] by
- Böhmová, J
- Vodička, R
- Lubušký, M
- Studničková, M
- Holusková, I
- Vrtěl, R
- Kratochvílová, R
- Frydrychová, M
- Krejčiříková, E
- Filipová, H
Producer: 20130924
In:
Ceska gynekologie vol. 78
Availability: No items available.
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19.
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Tumors overexpressing RNF168 show altered DNA repair and responses to genotoxic treatments, genomic instability and resistance to proteotoxic stress. [electronic resource] by
- Chroma, K
- Mistrik, M
- Moudry, P
- Gursky, J
- Liptay, M
- Strauss, R
- Skrott, Z
- Vrtel, R
- Bartkova, J
- Kramara, J
- Bartek, J
Producer: 20170901
In:
Oncogene vol. 36
Availability: No items available.
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20.
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Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. Online. [electronic resource] by
- Wang, Q
- Verhoef, S
- Tempelaars, A M
- Bakker, P L
- Vrtel, R
- Hesseling-Janssen, A L
- Nellist, M
- Oranje, A P
- Stroink, H
- Lindhout, D
- Halley, D J
- van den Ouweland, A M
Producer: 19990419
In:
Human mutation vol. 11
Availability: No items available.
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