GTR Home > Laboratories > Labor-MVZ Westmecklenburg

Labor-MVZ Westmecklenburg

GTR Lab ID: 320246, Last updated:2016-05-25
Annual Review past due read more

Personnel

Conditions and tests

  • Achondroplasia1 test
  • Acrocephalosyndactyly type I1 test
  • Alzheimer disease, type 11 test
  • Alzheimer disease, type 31 test
  • Alzheimer disease, type 41 test
  • Amelogenesis imperfecta - hypoplastic autosomal dominant - local1 test
  • Amelogenesis imperfecta, type IC1 test
  • Antithrombin III deficiency1 test
  • Autosomal recessive polycystic kidney disease1 test
  • Bartter syndrome type 31 test
  • Bartter syndrome, type 1, antenatal1 test
  • Bartter syndrome, type 2, antenatal1 test
  • Central core myopathy1 test
  • Chondrodysplasia punctata 2 X-linked dominant1 test
  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
  • Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A21 test
  • Congenital myopathy with fiber type disproportion1 test
  • Deficiency of butyrylcholine esterase1 test
  • Deficiency of steroid 11-beta-monooxygenase1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Dubin-Johnson syndrome1 test
  • Factor VII deficiency1 test
  • Familial hypokalemia-hypomagnesemia1 test
  • Fructose-biphosphatase deficiency1 test
  • GLUT1 deficiency syndrome 11 test
  • Hereditary angioedema type 31 test
  • Hereditary hemorrhagic telangiectasia type 11 test
  • Hereditary pancreatitis1 test
  • Huntington disease1 test
  • Hyperekplexia 12 tests
  • Hyperekplexia 31 test
  • Hypocalciuric hypercalcemia, familial, type 11 test
  • Hypochondroplasia1 test
  • Hypophosphatasia1 test
  • Leri-Weill dyschondrosteosis1 test
  • Malignant hyperthermia, susceptibility to, 11 test
  • Marfan syndrome1 test
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 11 test
  • Neuroferritinopathy1 test
  • Non-ketotic hyperglycinemia3 tests
  • Noonan syndrome 11 test
  • Oculopharyngeal muscular dystrophy1 test
  • Pancreatic agenesis and congenital heart disease1 test
  • Pfeiffer syndrome1 test
  • Polycystic kidney disease 21 test
  • Polycystic kidney disease, adult type1 test
  • PTEN hamartoma tumor syndrome1 test
  • Retinitis pigmentosa 191 test
  • Rett syndrome1 test
  • Rhizomelic chondrodysplasia punctata type 11 test
  • Rhizomelic chondrodysplasia punctata type 21 test
  • Seckel syndrome 11 test
  • Seckel syndrome 41 test
  • Short rib-polydactyly syndrome, Majewski type1 test
  • Stargardt disease 12 tests
  • Syndromic X-linked intellectual disability Lubs type1 test
  • Wilson disease1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Deletion/Duplication Testing
  • Prenatal testing
  • Custom Sequence Analysis
  • Carrier testing

List of certifications/licenses

Certifications

  • INSTAND, Number: 30098, Expiration date: 2016-03-31
  • RfB, Number: 7832052, Expiration date: 2016-03-31

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