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Om Kennedy Centret Organisation Medarbejdere Ledige stillinger Årsrapport m.m. Ventetider Her bor vi Kontakt Om kennedy.dk Links English - Limited version Laboratory analyses Laboratory pricelist Laboratory profile Exclusion of liability Research profile PKU, Fragile X and Rett syndrome Center for Fragilt X Center for PKU Center for Rett syndrom Forskning Synshandicap Øjenmalformationer og øjenudvikling Aniridi USHER syndrom Oculocutaneous albinism (OCA) AMD (aldersrelateret makuladegeneration) Autosomal dominant opticus atrofi Glaukom Mental retardering Gilles de Tourette Syndrom (GTS) Kromosomale ubalancer Fragilt X Down syndrom Kobberstofskiftet Menkes sygdom Funktionelle studier af ATP7A proteinet Udvikling af nye behandlingsmuligheder Epigenetik Maternel hypomethyleringssyndrom Aldersrelateret ændring i X-kromosom reaktivering PKU og beslægtede tilstande Phenylketonuri (PKU) Co-faktor BH4 og smerteforskning Familiær Dopa-responsiv dystoni Nyt fra forskningen Publikationer 2014 2013 2012 2011 2010 2009 2008 2007 2006 Tidligere publikationer Links Genetisk rådgivning Information Arvelig cancer rådgivning Sjældne kromosomafvigelser Lokationsnummer Priser Links - Genetisk rådgivning Laboratoriet English Nye analysetilbud Rekvisitioner Priser Vejledninger og downloads Kvalitetspolitik Synsregisteret Øjenklinikken Rekvisitioner Selvbetjening Links Privatlivspolitik

Sidst opdateret: 16/11 2017
Laboratory - Pricelist 2016
Contact laboratory

 

DKK 100 = 7,40 

Analyses specified by diagnosis

Dkk   

Euro  

1p36-deletion syndrome

Screening for mikrodeletion - MLPA*

2.100

284

Alagille syndrome

Screening for mikrodeletion - MLPA*

2.100

284

Albinism, oculocutaneous

Screening for mutation (Albinism NGS panel)*

15.513

2.096

Screening for mutation (OCA1/TYR) - sequencing*

6.032

815

Screening for mutation (OCA1/TYR) - MLPA*

2.100

284

Screening for mutation (OCA2/OCA2) - sequencing*

12.590

1.701

Screening for mutation (OCA2/OCA2) - MLPA*

2.100

284

Screening for mutation (OCA3/TYRP1) - sequencing*

6.723

909

Screening for mutation (OCA4/SLC45A2) (MATP) - sequencing*

6.723

909

Screening for mutation (OCA4/SLC45A2) - MLPA*

2.100

284

Screening for mutation (OCA7/C10orf11) - sequencing*

6.379

862

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043

Angelman syndrome

Methylation- & deletion analysis - MS-MLPA*

2.727

369

Uniparental disomy - UPD*

3.631

491

Aniridia

Screening for mikrodeletion (PAX6) - MLPA*

 2.100

284

Mutationsscreening (PAX6) - sequencing*

9.139

1.235

Analysis for a specified mutation*

4.840

654

Prenatal diagnosis*

7.716

1.043

Anterior segment defects

Screening for mutation (Anterior segment defects NGS panel)

18.616

2.516


ARX analysis

Screening for mutation (ARX) – sequencing*

6.379

862

Fragment size analysis (ARX)*

2.758

373

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043

Ataxi

Screening for mutation (Ataxi NGS panel)

18.616

2.516

Carrier analysis / analysis for specified mutation

4.840

654

Prenatal diagnosis

7.716

1.043

 

Ataxia-telangiectasia

Screening for mutation (ATM) (Ataxia-telangiectasia NGS panel)

15.513

2.096

Carrier analysis / analysis for specified mutation

4.840

654

Prenatal diagnosis

7.716

1.043


Axenfeld-Rieger syndrome

Screening for mutation (Axenfeld-Rieger, Peters anomali NGS panel)

15.513

2.096

Screening for mutation (PITX2) – sequencing*

6.032

815

Screening for mutation (FOXC1) – sequencing*

5.499

743

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043

Screening for microdeletion (PITX2, FOXC1), MPLA P054*

2.100

284

Bardet-Biedl Syndrome

Screening for mutation (BBS1 / BBS1) - sequencing

8.794

1.188

Screening for mutation (BBS2 / BBS2) - sequencing

9.829

1.328

Screening for mutation (BBS4 / BBS4) - sequencing

9.829

1.328

Screening for mutation (BBS6 / MKKS) - sequencing

7.069

955

Screening for mutation (BBS10 / BSS10) - sequencing

6.723

909

Carrier analysis

4.840

654

Beckwith Wiedemann syndrome

Methylation analysis - MS-MLPA*

2.727

369

Uniparental disomy - UPD*

3.631

491

Screening for mutation (CDKN1C) - sequencing*

5.687

769

BH4 mangel

Screening for mutation (BH4 NGS panel)

15.513

2.096

Screening for mutation (DHPR deficiency / QDPR) - sequencing*

6.732

909

Screening for mutation (GCH1 deficiency / GCH1) - sequencing*

6.379

862

Screening for mutation (PTS deficiency / PTS) - sequencing*

6.379

862

Screening for mutation (SPR deficiency / SPR) - sequencing*

5.342

622

Screening for mutation i (GCH1 / GCH1) - MLPA*

2.100

284

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043

Brankio-oto-renalt syndrome

Screening for mutation (BOR NGS panel)

5.435

734

Screening for mutation (EYA1) - sequencing 9.829

1.328

Screening for mutation (SIX1) - sequencing

6.032

815

Screening for mutation (SIX5) - sequencing

6.032

815

Screening for deletion/duplication (EYA1) - MLPA P153

2.100

284

Carrier analysis

4.840

654


CHARGE syndrome

Screening for mutation (CHD7) - sekventering 18.457

 2.4194

Screening for deletion/duplikation (CHD7) - MLPA P201

2.100

284

Carrier analysis

4.840

654

Prænatal diagnosis

7.716

1.043


Cornelia de Lange syndrome

Screening for mutation (CdLS NGS panel)

15.513

2.096

Screening for mutation (CdLS differential diagnosis NGS panel)

15.513

2.096

Screening for mutation (NIPBL) - MLPA 2.588

350

Carrier analysis / analysis for specified mutation

4.840

654

Prenatal diagnosis

7.716

1.043

 

Cri-du-chat syndrome

Microdeletion analysis - MLPA*

2.100

284

 

DiGeorge syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Dystonia

Screening for mutation (Dystoni NGS panel)

18.616

2.516

Screening for mutation (TH deficiency / Segawa syndrome / TH) - sequencing*

9.139

1.235

Screening for mutation (GCH1 deficiency / Segawa syndrome / GCH1) - sekventering*

6.379

862

Screening for mutation in both TH og GCH1 - MLPA* 2.100 284
Screening for mutation (SPR deficiency/SPR) - sequencing*

5.342

722

Screening for mutation (DYT1/TOR1A) - sequencing*

6.032

815

Screening for mutation (DYT1/TOR1A) (E302del)*

2.758

373

Screening for mutation (DYT6/THAP1) - sequencing*

5.166

722

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043

 

Ectodermal dysplasia 2, Clouston type

Screening for mutation (GJB6) – sequencing

5.342

 722

Carrier analysis

4.840

654

 

Fovea hypoplasi/nystagmus

Screening for mutation (Fovea hypoplasi/nystagmus NGS panel)

15.513

2.096


Fragilt X syndrome (FRAXA) (FMR1)

Analysis of expansion*

5.134

694

Prenatal diagnosis*

7.716

1.043

 

Glaucoma, primary open angle (POAG)

Screening for mutation (GLC1A / MYOC) - sequencing*

6.379

862

Screening for mutation (GLC1E / OPTN) - sequencing*

8.794

1.188

Screening for mutation (GLC1G / WDR36) - sequencing*

12.245

1.655

Analysis for a specified mutation*

4.840

654

 

Glaucoma, primary congenital (PCG)

Glaukom, primary congenital (CYP1B1) - sequencing*

6.379

862

Carrier analysis*

4.840

654

 

Prenatal diagnosis*

7.716

1.043

 

Hermansky Pudlak-, Chediak Higashi-, Griscelli syndrome

Screening for mutation (Hermansky Pudlak-, Chediak Higashi-, Griscelli syndrom NGS panel)

18.616

2.516

 

Hørenedsættelse og opticus atrofi m.m.

Screening for mutation (OPA1) - sequencing

13.971

1.888

Screening for mutation (ATP1A3) - sequencing (CAPOS syndrome)

12.245

 1.655

Screening for mutation (TIMM8A) - sequencing (Mohr Tranebjærg syndrome)

5.342

722

Screening for mutation (PRPS1), sequencing

6.501

879

Screening for deletion/duplication (OPA1) - MLPA  P229

2.100

284

Carrier analysis

4.840

654

 

Hørenedsættelse (non-syndromic)

Screening for mutation (GJB2 (exon 1 og 2) (Connexin 26)) sequencing

5.200

 703

Screening for del (GJB6-D13S1830) og del (GJB6-D13S1854)

1.275

 172

Screening for mutation (GJB2, DFNB1, Connexin 26), del (GJB6-D13S1830) og del (GJB6-D13S1854)

5.499

743

Screening for mutation (bashøretab/WFS1), sequencing

8.449

 1.142

Screening for mutation (høretab NGS panel A, ca. 35 gener, SLC26A4 inkluderet)

15.875

2.145

Screening for mutation (høretab NGS panel B, ca. 50 gener)

8.350

1.128

Screening for mutation (høretab NGS panel A+B samlet bestilling, ca. 85 gener)

20.575

2.780

Carrier analysis

4.840

654

Screening for mutation (STRC, deletion og sekv)

4.150

561

Screening for deletion/duplication (WFS1, GJB2, POU3F4) - MLPA P163

2.100

 284

Screening for mitokondriel hørenedsættelse, A1555G (MTRNR1)

1.722

 233

Screening for mitokondriel hørenedsættelse, A3243G (MTTL1)

1.722

 233

Screening for mitokondriel hørenedsættelse, A7445G (MTTS1)

1.722

 233

Screening for X-bunden hørenedsættelse (POU3F4) - sequencing

5.342

722

Screening for X-bunden hørenedsættelse (PRPS1) - sequencing

6.723

 909

Screening for X-bunden hørenedsættelse (SMPX) - sequencing

6.379

 862

Screening for mutation (TECTA), sequencing

12.245

 1.655

Screening for mutation (EYA4), sequencing

10.828

1.463

Screening for mutation (ACTG1), sequencing

6.379

 862

Screening for mutation (MYO6), sequencing

16.181

2.187

Andre gener og molekylærgenetiske analyser - individual pricing

 

Langer-Giedion syndrome

Screening for mikrodeletion - MLPA*

2.100

284

 

Lebers congenital amaurosis 2 (LCA2;RPE65)
Screening for mutation (RPE65) - sequencing*

9.139

1.235

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043

 

MECP2 duplication syndrome
Duplication analysis (MECP2) – MLPA*

2.100

284

Carrier analysis*

4.840

654

Prenatal diagnosis*

7.716

1.043


Menkes disease and Occipital Horn Syndrome

Screening for mutation (ATP7A) - sequencing*

12.245

1.655

Screening for mutation (ATP7A) - MLPA*

2.100

284

Carrier analysis*

4.840

654

 

Prenatal diagnosis*

 7.716

1.043


Mikrophtalmia / Anophtalmia
Screening for mutation (Mikroftalmi NGS panel)

 22.235

3.005

Screening for mutation (MCOPS3 / SOX2) - sequencing*

5.342

722

Screening for mutation (MCOPS5 / OTX2) - sequencing*

5.687

769

Screening for mutation (MCOPS3 / SOX2) - MLPA*

2.100

284

Screening for mutation (MCOPS5 / OTX2) - MLPA*

2.588

350

Carrier analysis*

4.840

654

 

Prenatal diagnosis*

7.716

1.043

Miller-Dieker syndrome

Microdeletion analysis - MLPA*

2.100

284

Mole, hydatidiform
Determination of ploidy*

1.536

208

QF-PCR Mola Hydatidosa - comparison*

885

120

Neurodegeneration med "Brain Iron Accumulation Disorders" (NBIA)

Screening for mutation (Movem disord NGS panel)

15.513

2.096

Carrier analysis / analysis for a specified mutation*

4.840

654

Prenatal diagnosis*

7.716

1.043


Optic atrophy, Kjer type
Analysis for Danish founder mutation (OPA1)*

2.758

373

Screening for mutation (OPA1) - sequencing*

13.971

1.888

Screening for mutation (OPA1) - MLPA*

2.100

284

Carrier analysis (founder mutation)*

2.758

373

Carrier analysis (analysis for other specified mutation)*

4.840

654

 

Prenatal diagnosis*

7.716

1.043


Parkinsons disease

Screening for mutation (Parkinsons disease NGS panel)

18.616

2.516

Carrier analysis / analysis for a specified mutation*

4.840

654

Prenatal diagnosis*

7.716

1.043

 

Pendred Syndrom / DFNB4

Screening for mutation (PDS NGS panel - SLC26A4, FOXI1, KCNJ10)

11.100

 1.500

Screening for mutation (SLC26A4 - alle exons, NGS eller Sanger)

10.235

 1.383

Screening for mutation (SLC26A4) - sequencing exon 2,4,6,8,10

9.685

 1.309

Screening for mutation (SLC26A4) - sequencing 16 rest exons

15.850

2.142

Screening for mutation (FOXI1) - sequencing

5.342

722

Screening for mutation (KCNJ10) - sequencing

5.076

 686

Carrier analysis

4.840

654

Screening for deletion/duplication (SLC26A4) - MLPA P280

2.100

284

 

PHARC syndrome

Screening for mutation (ABHD12) – sequencing

8.794

 1.188

Carrier analysis

4.840

654


Phenylketonuria (PKU)

Screening for mutation (PAH) - sequencing*

8.449

1.142

 

Screening for mutation (PAH) - MLPA*

2.100

284

 

Carrier analysis*

4.840

654

 

Prenatal diagnosis*

 7.716

1.036

 

Prader-Willi syndrome

Methylation- & deletion analysis - MS-MLPA*

2.727

369

Uniparental disomy (UPD)*

3.631

491

 

Rubinstein-Taybi syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Saethre-Chotzen syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Silver-Russell syndrome

Methylation- & deletion analysis - MS-MLPA*

2.727

369

 

Uniparental disomy (UPD, ME032)*

2.727

369

 

Smith-Magenis syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Sotos syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Tuberous sclerosis

Screening for mutation (TSC2) - sequencing*

18.457

2.494

Analysis for a specified mutation*

4.840

654

 

Prenatal diagnosis*

7.716

1.043

 

Tumor prædispositions syndrome

Screening for mutation (BAP1) - sekventering

8.794

1.188

 

USHER syndrome

Screening for mutation (CLRN1/USH3A genet), sequencing

6.032

815

Screening for mutation (USHER NGS, 13 gener)

12.150

1.642

Carrier analysis

4.840

654

Screening for deletion/duplication (USH2A), MLPA P361

2.100

284

Screening for deletion/duplication (USH2A), MLPA P362

2.100

284

Screening for deletion/duplication (PCDH15), MLPA P292

2.100

284

 

Waardenburg syndrome

Screening for mutation (WS NGS panel - SOX10, PAX3, SNAI2, MITF)

5.750

777

Screening for mutation (SOX10) - sequencing

5.687

769

Screening for mutation (PAX3) - sequencing

 7.169

969

Screening for mutation (SNAI2) - sequencing

5.342

722

Screening for mutation (MITF) - sequencing

7.169

969

Screening for deletion/duplication (PAX3, MITF) - MLPA P186

2.100

284

Carrier analysis

4.840

654


WAGR syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Williams syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Wilson syndrome

Screening for mutation (ATP7B) - sequencing*

11.555

1.561

Screening for mutation (ATP7B) - MLPA*

2.100

284

Carrier analysis*

4.840

654

 

Prenatal diagnosis*

7.716

1.043

 

Wolf syndrome

Microdeletion analysis - MLPA*

2.100

284

 

Wolfram syndrome (DIDMOAD)

Screening for mutation (WFS1) - sequencing

8.449

1.142

Screening for mutation (ZCD2) - sequencing

 5.342

722

Screening for deletion/duplication (WFS1) - MLPA P163

2.100

284

Carrier analysis

4.840

654

 

X-bunden mental retardation

Screening – (MRX) MLPA kit P106

2.100 284

 

X-inactivation

X-inactivation - PCR*

2.758

373


Analyses specified by methodology
Chromosome Microarray*

12.201

1.649

FISH, metaphases*

5.255

710

FISH, metaphases (prænatal)*

5.827

814

FISH, metaphases (postnatal)*

5.255

710

Subtelomeric MLPA*

2.100

284

Syndromic MLPA*

2.100

284

QF-PCR (prenatal or postnatal)*

885

120

QF-PCR Mola Hydatidosa - ploidibestemmelse*

1.590

215

QF-PCR Mola Hydatidosa - comparison*

885

120

Other QF-PCRs*

1.590

215

Mutation analysis, customized - sequencing (postnatal)*

7.377

997

Mutation analysis, customized – sequencing (prenatal)*

10.214

1.380

Deletion-/duplication analysis – qPCR (postnatal)*

2.837

383

  Deletion-/duplication analysis – qPCR (prenatal)*

4.256

575

Karyotyping / Chromosome analysis

Solid tissues (abortion, skin, other)*

5.280

714

Solid tissues (abortion, skin, other) - no growth*

2.526

342

Blood*

 3.050

412

Amniotic fluid*

5.460

738

Chorionic Villus Sample*

5.870

793

Metabolic analyses

Menkes copper analysis, cell retention dynamics*

15.928

2.152

  PKU B-Tyrosine og B Phenylalanine, quantitative*

285

39

Miscellaneous

Cell culturing*

2.451

331

EBV transformation of lymhocytes*

2.451

331

Shipping of samples (Denmark)

512

69

 

Shipping of samples (international)

738

100

* Accredited analyses

All prices on this web site are subject to change without notice. Whilst we make every effort to provide you the most accurate, up-to-date information, occasionally, one or more items on our web site may be mis-priced.
Updated 22nd of February 2016