MLPA® Kits

Please contact us, if you miss any mix definition.
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A, ME & R P001 to P019 P020 to P039 P040 to P059 P060 to P079 P080 to P099
P100 to P119 P120 to P139 P140 to P159 P160 to P179 P180 to P199 P200 to P219
P220 to P239 P240 to P259 P260 to P279 P280 to P299 P300 to P319 P320 to P339
P340 to P359 P360 to P379 P380 to P399 P400 to P419 P420 to P439 P440 to P459

Import of SALSA MLPA® kit descriptions via the SEQUENCE Pilot operation "Mixes [master file] / button [Import]".

Mix
Version
Date
Region
Application
Vs. 04
18-02-2010
 STS Xp22 Steroid Sulfatase gene (STS)
Vs. 04
30-10-2007
 GJB 1p35.1 (connexin 31), WFS1 4p16.1 (Wolframin) Hearing loss
Vs. 07
23-06-2008
 GJB 1p35.1 (connexin 31), WFS1 4p16.1 (Wolframin) Hearing loss
Vs. 08
30-07-2008
 GJB 1p35.1 (connexin 31), WFS1 4p16.1 (Wolframin) Hearing loss
Vs. 10
18-11-2009
 GJB 1p35.1 (connexin 31), WFS1 4p16.1 (Wolframin) Hearing loss
Vs. 11
04-01-2010
 GJB 1p35.1 (connexin 31), WFS1 4p16.1 (Wolframin) Hearing loss
Vs. 13
10-11-2011
 GJB 1p35.1 (connexin 31), WFS1 4p16.1 (Wolframin) Hearing loss
Vs. 23
11-06-2008
 IDS Xq28 Mucopolysaccharidosis type II, or Hunter syndrome
Vs. 08
01-05-2010
 IDS Xq28 Mucopolysaccharidosis type II, or Hunter syndrome
Vs. 10
21-11-2006
 SPG3A 14q21, SPAST 2p22 Spastic paraplegia, hereditary (HSP)
Vs. 18
22-07-2008
 SPG3A 14q21, SPAST 2p22 Spastic paraplegia, hereditary (HSP)
Vs. 21
23-10-2011
 SPG3A 14q21, SPAST 2p22 Spastic paraplegia, hereditary (HSP)
Vs. 04
09-12-2009
 KCNQ2 20q13.33 Benign familial neonatal convulsion (BFNC)
Vs. 05
11-07-2011
 KCNQ2 20q13.33 Benign familial neonatal convulsion (BFNC)
Vs. 04
04-03-2007
 DSP 6p24, PKP2 12q11.21 Arrhythmogenic right ventricular cardiomyopathy (ARVC)
Vs. 06
16-05-2011
 DSP 6p24, PKP2 12q11.21 Arrhythmogenic right ventricular cardiomyopathy (ARVC)
Vs. 02
18-07-2006
 RET 10q11.2, ZFHX1B 2q22.3, EDN3 20q13.3 and GDNF 5q13.2 Hirschsprung disease, or Aganglionic Megacolon
Vs. 06
25-09-2008
 RET 10q11.2, ZFHX1B 2q22.3, EDN3 20q13.3 and GDNF 5q13.2 Hirschsprung disease, or Aganglionic Megacolon
Vs. 05
25-06-2008
 APP 21q21.3 Alzheimer disease, early-onset
Vs. 06
29-12-2008
 APP 21q21.3 Alzheimer disease, early-onset
Vs. 09
10-03-2008
 various genes Tumours
Vs. 01
18-09-2008
 various genes Tumours
Vs. 03
29-05-2009
 CAPN3 15q15.1 Limb girdle muscular dystrophy 2A (LGMD2A)
Vs. 05
04-11-2011
 CAPN3 15q15.1 Limb girdle muscular dystrophy 2A (LGMD2A)
Vs. 01
09-08-2006
 CASR 3q13 Hypocalciuric Hypercalcemia, familial
Vs. 03
09-05-2009
 CASR 3q13 Hypocalciuric Hypercalcemia, familial
Vs. 04
26-11-2010
 CASR 3q13 Hypocalciuric Hypercalcemia, familial
Vs. 01
24-05-2006
 FVIII Xq28 Haemophilia A, x-linked
Vs. 03
11-01-2007
 FVIII Xq28 Haemophilia A, x-linked
Vs. 04
26-06-2007
 FVIII Xq28 Haemophilia A, x-linked
Vs. 06
04-08-2008
 FVIII Xq28 Haemophilia A, x-linked
Vs. 07
04-02-2009
 FVIII Xq28 Haemophilia A, x-linked
Vs. 08
10-06-2009
 FVIII Xq28 Haemophilia A, x-linked
Vs. 09
03-05-2010
 FVIII Xq28 Haemophilia A, x-linked
Vs. 07
21-06-2010
 GLI3 7p13, HOXD13 2q31, ROR2 9q22 Limb malformations
Vs. 09
12-09-2011
 GLI3 7p13, HOXD13 2q31, ROR2 9q22 Limb malformations
Vs. 11
10-01-2012
 GLI3 7p13, HOXD13 2q31, ROR2 9q22 Limb malformations