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Molecular Genetics Laboratory - Diagnostics Genetics

GTR Lab ID: 17510, Last updated:2017-05-10
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Personnel

  • Director: Donald Love, PhD, Lab Director
    Phone: +64-9-307-4949 ext 22013
    Fax: +64-9-307-4939
    Email: donaldl@adhb.govt.nz
  • Alice George, BSc (Hons), Technical Head
    Phone: +64-9-307-4949 ext 22010
    Fax: +64-9-307-2826
    Email: aliceg@adhb.govt.nz
  • Edward Atack, BSc, Staff
    Phone: 0064 307 4949 x22014
    Email: edwarda@adhb.govt.nz

Conditions and tests

  • Achondroplasia1 test
  • Adrenoleukodystrophy1 test
  • Albright's hereditary osteodystrophy1 test
  • Angelman syndrome1 test
  • Becker muscular dystrophy1 test
  • Breast cancer, susceptibility to2 tests
  • Breast-ovarian cancer, familial 13 tests
  • Breast-ovarian cancer, familial 23 tests
  • Brugada syndrome1 test
  • Cardiomyopathy1 test
  • Carnitine palmitoyltransferase I deficiency1 test
  • Catecholaminergic polymorphic ventricular tachycardia1 test
  • Charcot-Marie-Tooth disease, type 4D1 test
  • Charcot-Marie-Tooth disease, type IA1 test
  • Citrullinemia type I1 test
  • Classical galactosemia, homozygous Duarte-type1 test
  • Cowden syndrome 11 test
  • Crouzon syndrome with acanthosis nigricans1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Duchenne muscular dystrophy1 test
  • Dystonia 5, Dopa-responsive type1 test
  • Dystonia 6, torsion1 test
  • Dystrophinopathies1 test
  • Fabry disease1 test
  • Familial adenomatous polyposis 11 test
  • Familial hypoplastic, glomerulocystic kidney3 tests
  • Familial medullary thyroid carcinoma1 test
  • Fragile X syndrome1 test
  • Hereditary breast and ovarian cancer syndrome3 tests
  • Hereditary diffuse gastric cancer1 test
  • Hereditary liability to pressure palsies1 test
  • Hereditary Paraganglioma-Pheochromocytoma Syndromes1 test
  • Holocarboxylase synthetase deficiency1 test
  • Huntington's chorea1 test
  • Hyperinsulinemic hypoglycemia familial 31 test
  • Hypochondroplasia1 test
  • Kugelberg-Welander disease1 test
  • Lissencephaly 11 test
  • Long QT syndrome1 test
  • Maturity onset diabetes mellitus in young1 test
  • Maturity-onset diabetes of the young, type 12 tests
  • Maturity-onset diabetes of the young, type 22 tests
  • Maturity-onset diabetes of the young, type 32 tests
  • McCune-Albright syndrome1 test
  • Muenke syndrome1 test
  • Multiple endocrine neoplasia, type 21 test
  • Myoclonic dystonia1 test
  • Non-ketotic hyperglycinemia1 test
  • Osteogenesis imperfecta, type XI1 test
  • Paraganglioma and gastric stromal sarcoma1 test
  • Paragangliomas 11 test
  • Paragangliomas 31 test
  • Paragangliomas 41 test
  • Pheochromocytoma1 test
  • Prader-Willi syndrome1 test
  • Pseudohypoparathyroidism1 test
  • Pseudopseudohypoparathyroidism1 test
  • PTEN hamartoma tumor syndrome1 test
  • Rett syndrome1 test
  • Severe neonatal-onset encephalopathy with microcephaly1 test
  • short QT syndrome1 test
  • Spastic paraplegia 4, autosomal dominant1 test
  • Spinal muscular atrophy1 test
  • Steinert myotonic dystrophy syndrome1 test
  • Subcortical band heterotopia1 test
  • Thanatophoric dysplasia type 11 test
  • Von Hippel-Lindau syndrome1 test
  • Werdnig-Hoffmann disease1 test
  • Wilson disease1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Mutation Confirmation

List of certifications/licenses

Certifications

  • ISO15189, Number: 204, Expiration date: 2017-03-11

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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