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Univ. of Coruña. Campus Elviña. Edif. C. Educac. (
A Coruña, E-15071, Spain
Phone: 34-981-167000 (1709) Fax: 34-981-167153 Please notice: This entry hasn't been updated by the submitting company for more than 2 years. It could be possible that this company doesn't longer exists.
Description:
We carried out a series of tests of diagnostic application which have been developed in our lab.These tests would be of great utility in hands of oncologists, pediatricians, neurologists, clinical, and geneticists. We are an Unit of Genetics and Molecular Diagnosis of the University of The Coruña and we acted under the help of the Galician Institute of Molecular Medicine. Our main objective is in elevating the quality of the medical attention offered to the population and promote the use, handling and domain of new diagnostic procedures that will dominate the medicine of the next millennium, the Molecular Medicine. If you are looking for a genetic laboratory which be able to help you in order to obtain an highly ACCURATE, FAST, and non-expensive molecular genetic diagnosis we invite you to contact us, we could help you.
CODE////////METHOD///////////////////////US DOLLAR PRIZES
MM.1////////ONCOGENETICS MM.1.1////////"Translocation t(9;22)"///////////254 MM.1.10////////APC/////////////////////////////1330 MM.1.11////////VHL//////////////////////////////300 MM.1.12////////N-myc////////////////////////////150 MM.1.13////////C-myc////////////////////////////150 MM.1.14////////HER-2(erbB2)/////////////////////150 MM.1.15////////K-ras////////////////////////////307 MM.1.16////////p53//////////////////////////////240 MM.1.17////////Microsatellite instab.///////////240 MM.1.2////"PML-RAR(alfa). Translocation t(15;17)" 254 MM.1.3////"TEL-AML1. Translocation t(12;21)"/////254 MM.1.4////////"Translocation t(14;18)"///////////150 MM.1.5////////"Translocation t(11;14)"///////////150 MM.1.6////////"Translocation t(8;21)"////////////255 MM.1.7////////Rearrangement IgH /////////////////150 MM.1.8////////Rearrangement TCR//////////////////150 MM.1.9////////BRCA1 and BRCA2///////////////////1700
MM.2////////GENETIC DISORDERS-NEUROGENETICS MM.2.1////Duchenne-Becker Muscular Dystrophy/////255 MM.2.10////////21-hydroxilase////////////////////370 MM.2.11////////GH Receptor///////////////////////540 MM.2.12////////Gs-alfa (GNSA1)///////////////////540 MM.2.13a////////Achondroplasia///////////////////200 MM.2.13b////////Hypochondroplasia////////////////200 MM.2.14////////Muir-Torre///////////////////////1400 MM.2.15////////MEN///////////////////////////////150 MM.2.16////////Hemocromatosis////////////////////200 MM.2.17////////Cystic Fibrosis///////////////////200 MM.2.18////////Hemoglobinopathies////////////////240 MM.2.19////////Di George Syndrome////////////////270 MM.2.2////////Retinosis Pigmentaria//////////////500 MM.2.20////////Noonan Syndrome///////////////////270 MM.2.21////////Fragile X Syndrome////////////////150 MM.2.22////////Huntington´s Disease//////////////250 MM.2.23////////Enfermedad de Kennedy/////////////150 MM.2.24////////SCA1//////////////////////////////150 MM.2.25////////Dentatorub.-Pallidolyusian Atr.///150 MM.2.26////////Machado-Joseph Dis. (MJD, SCA3)///150 MM.2.27////////Myotonic Dystrophy (DM)///////////150 MM.2.28////////Friedreich Ataxia (FRDA)//////////150 MM.2.29////////Spinocerebellar ataxia 2 (SCA2)///150 MM.2.3///Linkage to ARPKD. Polycystic kidney/////340 MM.2.30////////Glaucoma//////////////////////////150 MM.2.4////////Linkage to LDLR////////////////////270 MM.2.5////////Linkage to NPC1////////////////////340 MM.2.6////////Mitochondrial DNA//////////////////340 MM.2.7////////TNF////////////////////////////////200 MM.2.8////////CYP11B1-CYP11B2////////////////////340 MM.2.9////////11-ß-hidroxilase//////////////////1400
MM.3///////////OTHERS MM.3.1////////Monozygocism///////////////////////450 MM.3.2////////Chimerism (Transplante de médula)//450 MM.3.3////////Chromosoma Y (Molecular Analysis)//450 MM.3.a////////Charcot Marie Tooth 1A/////////////450 MM.3.b////////Tay-Sachs//////////////////////////500 MM.3.c////////Prader-Willi Syndrome//////////////300 MM.3.d.///////Angelmann Syndrome/////////////////300
Last update of this entry: before October 1999.
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