Medical / Clinical Laboratory

Molecular Diagnostics / PCR

Accredited laboratories offering molecular diagnostics / pcr testing services across Europe.

536 Accredited labs
10 Countries

Showing 426–450 of 476 labs

DAkkS D-ML-13220-02-00 Homburg, DE
freies Hämoglobin Erythrozyten Hämatokrit Hämoglobin Kleines Differential-Blutbild + 3 more
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DAkkS D-ML-13220-03-00 Homburg, DE
CACNA1A A>T rs17580 G>A rs28929474 FIB/HS: PNPLA3 p. I148M c.617 rs738409 + 3 more
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Zentrallabor

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DAkkS D-ML-13220-01-01 Homburg, DE
Urinsediment Lamotrigin HbA1c Erythrozyten Aripiprazol + 3 more
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DAkkS D-ML-13155-04-00 Greifswald, DE
Familiäre Adenomatöse Polyposis Syndrome (APC, MUTYH) STK11, SMAD4 ), TruRisk® -Panel [SNV, CN Familiäre Polyposis-Syndrome [FAP] (APC, MUTYH) + 3 more
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DAkkS D-ML-13155-05-00 Greifswald, DE
Heparin-induzierte Plättchenantikörper PF4-induzierte Plättchenantikörper Thrombusstabilität Plättchenfunktion (ATP-Freisetzung) + 3 more
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DAkkS D-ML-13161-02-00 Göttingen, DE
angeborener Chromosomensatz Molybdän-Cofaktor Defizienz (MOCS1, MOCS2) Fragiles X-Syndrom: FMR1 Spinocerebellare Ataxie (SCA) + 3 more
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DAkkS D-ML-13161-01-00 Göttingen, DE
Thrombozytenaggregation Born VerschluĂźzeit Kollagen/ADP VerschluĂźzeit Kollagen/Adrenalin 6-Methyl-Mercaptopurinnukleotide + 3 more
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DAkkS D-ML-13161-05-00 Göttingen, DE
Thrombozytenaggregation Born VerschluĂźzeit Kollagen/ADP VerschluĂźzeit Kollagen/Adrenalin 6-Methyl-Mercaptopurinnukleotide + 3 more
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DAkkS D-ML-13161-06-00 Göttingen, DE
angeborener Chromosomensatz Molybdän-Cofaktor Defizienz (MOCS1, MOCS2) Fragiles X-Syndrom: FMR1 Spinocerebellare Ataxie (SCA) + 3 more
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DAkkS D-ML-13193-04-00 Rostock, DE
alpha-Aminobuttersäure Mianserin Arginin Asparagin Asparaginsäure + 3 more
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DAkkS D-ML-13193-01-00 Rostock, DE
Candida spp.-Antikörper Cardiolipin-Antikörper Meningitiserreger-Ag (E. coli Staphylococcus aureus Treponema pallidum-Antikörper + 3 more
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DAkkS D-ML-13193-03-01 Rostock, DE
Granulozytäre Antikörper (Screening und Differenzierung) HLA spezifische Antikörper B-Streptokokken (Screening) Ektoparasiten (Differenzierung) + 3 more
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DAkkS D-ML-13258-01-01 Mainz, DE
angeborener Chromosomensatz Silver-Russell-Syndrom: H19, KCNQ1OT1 MEST Deletion; Angelman-Syndrom + 3 more
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DAkkS D-ML-13258-03-00 Mainz, DE
5-Hydroxyindolessigsäure Amitriptylin/Nortriptylin Cyclosporin A Gesamt-Itraconazol Metanephrine, Normetanephrine + 3 more
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DAkkS D-ML-13258-05-00 Mainz, DE
geringe Auflösung hohe Auflösung low resolution Thrombozytenantigene Molekulargenetische + 3 more
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VDZ Service

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DAkkS D-PL-16069-01-01 DĂĽsseldorf, DE
DIN 1048-1 DIN 1048-5 DIN 1164-11 DIN 66133 DIN EN 196-3 + 3 more
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DAkkS D-PL-18403-01-01 DĂĽsseldorf, DE
DIN 1048-5 DIN CEN/TS 12390-9 DIN EN 62196-1: 2015 DIN EN 196-3 DIN EN 196-6 + 3 more
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DAkkS D-PL-19465-01-00 Darmstadt, DE
Myopathie, Nemaline (TyP1, 3-10: ASTM E 23-18 ASTM D 1322 Toxizität UGT1A1-Gen rs3064744, rs414832 DIN EN 1789 + 3 more
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DAkkS D-PL-11105-01-01 Sinzheim, DE
dbSNP rs1801133 und rs1801131 EN ISO 11925-2 DIN V ENV 807 (p.Ala222Val); dbSNP rs1801133 DIN CEN/TS 15082
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DAkkS D-ML-22115-01-00 Berlin, DE
AB0-D Blutgruppentest (kurz) AB0-D Blutgruppentest (lang) RhCE-Blutgruppentest Kell-Blutgruppentest, (K) serologische Phänotypisierung + 3 more
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DAkkS D-PL-17674-02-02 Garching-HochbrĂĽck, DE
DIN EN ISO 5667-1 (A 4) DIN 38402-A 13 DIN ISO 5667-5 (A 14) DIN EN ISO 5667-3 (A 21) DIN EN ISO 19458 (K 19) + 3 more
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DAkkS D-ML-13013-01-00 Chemnitz, DE
Thrombozytenfunktion Ristocetin) Thrombozytenaggregation Arachidonsäure, Epinephrin, Kollagen, Ri 17-alpha-Hydroxy-Progesteron + 3 more
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DAkkS D-ML-13117-01-00 Regensburg, DE
angeborener Chromosomensatz 22q11.2-Mikrodeletionssyndrom (22q11.2) Kopienzahlveränderungen (Regionen laut MLPA-Kit) + 3 more
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DAkkS D-ML-21320-01-01 TĂĽbingen, DE
angeborener Chromosomensatz (Imbalancen im Genom, Duplikationen, Del Chromosomenstörung XYY, XXYY Rhesusfaktor + 3 more
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DAkkS D-ML-22408-01-01 TĂĽbingen, DE
Thrombozytenaggregation (Collagen, Epinephrin, Ristocetin, Trap- (Ionophore, ADP, Kollagen) ASPI, Collagen, TRAP-6) Verschlusszeitbestimmung + 3 more
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