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GTR Home > Laboratories > Integrated Genetics Westborough

Integrated Genetics Westborough

GTR Lab ID: 500094, Last updated:2024-01-13

Personnel

  • Director: Natalia Leach, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Director: Robert Pyatt, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Director: Jennifer Reiner, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Director: Zena Wolf, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Director: Winnie Xin, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Director: Zhaoqing Zhou, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Director: Hui Zhu, PhD, ABMGG Board Certified, Diplomate of the American Board of Medica, Lab Director
  • Karen Giger, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 800-255-7357
    Email: gigerk@labcorp.com
  • Jennifer Teicher, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 800-255-7357
    Email: jennifer.teicher@integratedgenetics.com

Conditions and tests

  • 3-M syndrome6 tests
  • 3-Methylglutaconic aciduria type 26 tests
  • 3-Methylglutaconic aciduria type 36 tests
  • Abetalipoproteinaemia8 tests
  • Achondrogenesis, type IB9 tests
  • Achromatopsia8 tests
  • Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins6 tests
  • Acyl-CoA oxidase deficiency6 tests
  • Adams-Oliver syndrome4 tests
  • Adrenoleukodystrophy8 tests
  • Agenesis of the corpus callosum with peripheral neuropathy8 tests
  • Aicardi Goutieres syndrome8 tests
  • Allan-Herndon-Dudley syndrome6 tests
  • alpha Thalassemia10 tests
  • Alpha thalassemia-X-linked intellectual disability syndrome6 tests
  • Alpha-N-acetylgalactosaminidase deficiency type 18 tests
  • Alport syndrome8 tests
  • Alstrom syndrome8 tests
  • Apolipoprotein A-I deficiency5 tests
  • Apolipoprotein c-III deficiency4 tests
  • Arginase deficiency6 tests
  • Argininosuccinate lyase deficiency9 tests
  • Arrhythmogenic right ventricular cardiomyopathy5 tests
  • Arterial tortuosity syndrome7 tests
  • Arteriohepatic dysplasia4 tests
  • Aspartylglucosaminuria9 tests
  • Ataxia-telangiectasia syndrome8 tests
  • Atelosteogenesis type II9 tests
  • Atransferrinemia8 tests
  • Atrial fibrillation4 tests
  • Atrial septal defect4 tests
  • Autism spectrum disorder - epilepsy - arthrogryposis syndrome8 tests
  • Autosomal recessive axonal neuropathy with neuromyotonia6 tests
  • Autosomal recessive congenital ichthyosis6 tests
  • Autosomal recessive limb-girdle muscular dystrophy type 2M8 tests
  • Autosomal recessive polycystic kidney disease3 tests
  • Bardet-Biedl syndrome9 tests
  • Bartter syndrome6 tests
  • Batten-Turner congenital myopathy7 tests
  • Becker muscular dystrophy11 tests
  • beta Thalassemia10 tests
  • Beta-D-mannosidosis8 tests
  • Bifunctional peroxisomal enzyme deficiency8 tests
  • Biotin-responsive basal ganglia disease8 tests
  • Biotinidase deficiency8 tests
  • Bloom syndrome10 tests
  • Brittle cornea syndrome6 tests
  • Brugada syndrome4 tests
  • Cantu syndrome, KCNJ8 related4 tests
  • Cardio-facio-cutaneous syndrome7 tests
  • Carnitine acylcarnitine translocase deficiency8 tests
  • Carnitine palmitoyl transferase 1A deficiency6 tests
  • Carnitine palmitoyltransferase II deficiency9 tests
  • Carpenter syndrome6 tests
  • Catecholaminergic polymorphic ventricular tachycardia4 tests
  • Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency6 tests
  • Centronuclear myopathy6 tests
  • Cerebellar hypoplasia6 tests
  • Cerebral creatine deficiency syndrome9 tests
  • CHARGE syndrome4 tests
  • Charlevoix-Saguenay spastic ataxia8 tests
  • Cholestanol storage disease8 tests
  • Chorea-acanthocytosis6 tests
  • Chronic granulomatous disease6 tests
  • Chédiak-Higashi syndrome6 tests
  • Ciliopathy8 tests
  • Citrullinemia8 tests
  • Coats plus syndrome6 tests
  • Cockayne syndrome6 tests
  • Coffin-Lowry syndrome6 tests
  • Cohen syndrome8 tests
  • Cold-induced sweating syndrome6 tests
  • Cold-induced sweating syndrome 16 tests
  • Combined deficiency of sialidase AND beta galactosidase8 tests
  • Combined malonic and methylmalonic acidemia6 tests
  • Combined molybdoflavoprotein enzyme deficiency6 tests
  • Combined oxidative phosphorylation deficiency6 tests
  • Combined pituitary hormone deficiencies, genetic form6 tests
  • Complex V deficiency6 tests
  • Congenital adrenal hyperplasia8 tests
  • Congenital adrenal hypoplasia6 tests
  • Congenital adrenal hypoplasia, X-linked2 tests
  • Congenital amegakaryocytic thrombocytopenia6 tests
  • Congenital contractural arachnodactyly4 tests
  • Congenital defect of folate absorption6 tests
  • Congenital disorder of deglycosylation6 tests
  • Congenital disorder of glycosylation10 tests
  • Congenital generalized lipodystrophy6 tests
  • Congenital hyperammonemia, type I8 tests
  • Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome6 tests
  • Congenital myasthenic syndrome8 tests
  • Congenital myotonia1 test
  • Corneal dystrophy-perceptive deafness syndrome6 tests
  • Cortical dysplasia-focal epilepsy syndrome6 tests
  • Costello syndrome7 tests
  • Cryptophthalmos syndrome8 tests
  • Cutis laxa7 tests
  • Cutis laxa, autosomal recessive, type 1B4 tests
  • Cystic fibrosis15 tests
  • Cystinosis8 tests
  • Danon disease7 tests
  • Deficiency of 2-methylbutyryl-CoA dehydrogenase6 tests
  • Deficiency of acetyl-CoA acetyltransferase9 tests
  • Deficiency of alpha-mannosidase8 tests
  • Deficiency of aromatic-L-amino-acid decarboxylase6 tests
  • Deficiency of hyaluronoglucosaminidase6 tests
  • Deficiency of hydroxymethylglutaryl-CoA lyase8 tests
  • Deficiency of mevalonate kinase8 tests
  • Dent disease6 tests
  • Diastrophic dysplasia9 tests
  • DiGeorge syndrome4 tests
  • Dihydropyrimidine dehydrogenase deficiency8 tests
  • Dilated cardiomyopathy 3B11 tests
  • Distal spinal muscular atrophy6 tests
  • Donnai-Barrow syndrome8 tests
  • Duchenne muscular dystrophy11 tests
  • Dyskeratosis congenita6 tests
  • Early infantile epileptic encephalopathy with suppression bursts8 tests
  • Ehlers-Danlos syndrome4 tests
  • Ehlers-Danlos syndrome due to tenascin-X deficiency8 tests
  • Ehlers-Danlos syndrome, dermatosparaxis type8 tests
  • Ellis-van Creveld syndrome8 tests
  • Emery-Dreifuss muscular dystrophy7 tests
  • Epidermolysis bullosa dystrophica8 tests
  • Ethylmalonic encephalopathy8 tests
  • Fabry disease9 tests
  • Familial amyloid neuropathy5 tests
  • Familial aortopathy4 tests
  • Familial cardiomyopathy5 tests
  • Familial dysautonomia10 tests
  • Familial hemophagocytic lymphohistiocytosis8 tests
  • Familial hypercholesterolemia5 tests
  • Familial hyperinsulinism9 tests
  • Familial isolated deficiency of vitamin E8 tests
  • Familial Mediterranean fever9 tests
  • Familial thoracic aortic aneurysm and aortic dissection4 tests
  • Fanconi anemia10 tests
  • Fragile X syndrome14 tests
  • Fucosidosis2 tests
  • Galactosemia10 tests
  • Galactosylceramide beta-galactosidase deficiency8 tests
  • Gaucher disease10 tests
  • Glucocorticoid deficiency with achalasia6 tests
  • Glutaric aciduria, type 18 tests
  • Glycogen phosphorylase kinase deficiency6 tests
  • Glycogen storage disease type III7 tests
  • Glycogen storage disease, type I9 tests
  • Glycogen storage disease, type II9 tests
  • Glycogen storage disease, type IV8 tests
  • Glycogen storage disease, type V6 tests
  • Glycogen storage disease, type VII6 tests
  • GM1 gangliosidosis8 tests
  • GNE myopathy6 tests
  • GNPTG-mucolipidosis6 tests
  • GRACILE syndrome8 tests
  • Hb SS disease1 test
  • Hemophilia B, Factor IX Deficiency6 tests
  • Hepatic veno-occlusive disease-immunodeficiency syndrome6 tests
  • Hereditary acrodermatitis enteropathica6 tests
  • Hereditary factor IX deficiency disease2 tests
  • Hereditary fructosuria9 tests
  • Hereditary hemorrhagic telangiectasia4 tests
  • Hereditary insensitivity to pain with anhidrosis6 tests
  • Hereditary pulmonary alveolar proteinosis8 tests
  • Hereditary spastic paraplegia6 tests
  • Hermansky-Pudlak syndrome8 tests
  • Histiocytic medullary reticulosis7 tests
  • Holocarboxylase synthetase deficiency8 tests
  • Holt-Oram syndrome4 tests
  • Homocystinuria10 tests
  • HSD10 mitochondrial disease6 tests
  • Hyaline fibromatosis syndrome6 tests
  • Hydrocephalus, nonsyndromic, autosomal recessive 18 tests
  • Hydrolethalus syndrome7 tests
  • Hyper-IgM syndrome type 16 tests
  • Hyperammonemia, type III6 tests
  • Hyperimmunoglobulin M syndrome6 tests
  • Hyperlipidemia4 tests
  • Hyperlipoproteinemia, type I6 tests
  • Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome6 tests
  • Hyperphenylalaninemia due to tetrahydrobiopterin deficiency6 tests
  • Hypertrichotic osteochondrodysplasia Cantu type4 tests
  • Hypertriglyceridemia4 tests
  • Hypertrophic cardiomyopathy4 tests
  • Hypohidrotic ectodermal dysplasia6 tests
  • Hypomyelination and Congenital Cataract6 tests
  • Hypophosphatasia9 tests
  • Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly6 tests
  • Inherited glutathione synthetase deficiency8 tests
  • Insulin-dependent diabetes mellitus secretory diarrhea syndrome6 tests
  • Intellectual disability6 tests
  • Isovaleryl-CoA dehydrogenase deficiency7 tests
  • Jeune thoracic dystrophy8 tests
  • Joubert syndrome and related disorders9 tests
  • Junctional epidermolysis bullosa8 tests
  • Juvenile hemochromatosis6 tests
  • Juvenile retinoschisis8 tests
  • L1 syndrome7 tests
  • LAMA2-related muscular dystrophy6 tests
  • Leber congenital amaurosis6 tests
  • Legius syndrome7 tests
  • Leigh syndrome8 tests
  • Lethal arthrogryposis-anterior horn cell disease syndrome6 tests
  • Limb-girdle muscular dystrophy8 tests
  • Loeys-Dietz syndrome5 tests
  • Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency8 tests
  • Long QT syndrome4 tests
  • Lysinuric protein intolerance6 tests
  • Lysosomal acid lipase deficiency7 tests
  • Macular corneal dystrophy6 tests
  • Maple syrup urine disease9 tests
  • Marfan syndrome5 tests
  • Meckel-Gruber syndrome9 tests
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency9 tests
  • Meester-Loeys syndrome4 tests
  • Megalencephalic leukoencephalopathy with subcortical cysts 18 tests
  • Menkes kinky-hair syndrome6 tests
  • Metachromatic leukodystrophy9 tests
  • Metaphyseal chondrodysplasia, McKusick type8 tests
  • Methylcrotonyl-CoA carboxylase deficiency8 tests
  • Methylmalonic acidemia9 tests
  • Methylmalonic aciduria and homocystinuria9 tests
  • MHC class II deficiency6 tests
  • Microcephaly, normal intelligence and immunodeficiency8 tests
  • Mitochondrial complex deficiency8 tests
  • Mitochondrial complex I deficiency6 tests
  • Mitochondrial DNA depletion syndrome 16 tests
  • Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)6 tests
  • Mitochondrial DNA depletion syndrome, myopathic form6 tests
  • Mitochondrial trifunctional protein deficiency6 tests
  • Mucolipidosis type II9 tests
  • Mucolipidosis type IV10 tests
  • Mucopolysaccharidosis type 19 tests
  • Mucopolysaccharidosis type 68 tests
  • Mucopolysaccharidosis type 78 tests
  • Mucopolysaccharidosis, MPS-II8 tests
  • Mucopolysaccharidosis, MPS-IV-A8 tests
  • Mucopolysaccharidosis, MPS-IV-B8 tests
  • Multiple acyl-CoA dehydrogenase deficiency6 tests
  • Multiple epiphyseal dysplasia type 49 tests
  • Multiple pterygium syndrome6 tests
  • Multiple sulfatase deficiency8 tests
  • Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 48 tests
  • Myopathy, lactic acidosis, and sideroblastic anemia6 tests
  • Nemaline myopathy9 tests
  • Nephrogenic diabetes insipidus6 tests
  • Nephrotic syndrome9 tests
  • Neurodegeneration with brain iron accumulation6 tests
  • Neurofibromatosis, type 14 tests
  • Neuronal ceroid lipofuscinosis8 tests
  • Niemann-Pick disease, type A10 tests
  • Niemann-Pick disease, type B10 tests
  • Niemann-Pick disease, type C8 tests
  • Non-ketotic hyperglycinemia8 tests
  • Nonsyndromic genetic hearing loss8 tests
  • Noonan syndrome7 tests
  • Noonan syndrome with multiple lentigines7 tests
  • Oculocutaneous albinism8 tests
  • Opitz G/BBB syndrome8 tests
  • Ornithine aminotransferase deficiency6 tests
  • Ornithine carbamoyltransferase deficiency9 tests
  • Osteogenesis imperfecta6 tests
  • Osteopetrosis6 tests
  • Pelizaeus-Merzbacher disease8 tests
  • Pendred syndrome8 tests
  • Peroxisome biogenesis disorder8 tests
  • Phenylketonuria9 tests
  • PHGDH deficiency8 tests
  • Pigmentary pallidal degeneration6 tests
  • POLG-Related Spectrum Disorders8 tests
  • Polycystic kidney disease6 tests
  • Polyglandular autoimmune syndrome, type 18 tests
  • Polymicrogyria6 tests
  • Pontoneocerebellar hypoplasia8 tests
  • Primary congenital glaucoma6 tests
  • Primary dilated cardiomyopathy4 tests
  • Primary hyperoxaluria9 tests
  • Primary microcephaly8 tests
  • Progressive familial intrahepatic cholestasis6 tests
  • Progressive pseudorheumatoid dysplasia6 tests
  • Propionic acidemia8 tests
  • Pseudocholinesterase deficiency6 tests
  • Pyknodysostosis6 tests
  • Pyridoxal phosphate-responsive seizures6 tests
  • Pyridoxine-dependent epilepsy6 tests
  • Pyruvate carboxylase deficiency6 tests
  • Pyruvate dehydrogenase complex deficiency8 tests
  • Pyruvate dehydrogenase E3 deficiency9 tests
  • Qualitative or quantitative defects of dystrophin11 tests
  • Renal carnitine transport defect8 tests
  • Renal tubular acidosis with progressive nerve deafness6 tests
  • Retinitis pigmentosa9 tests
  • Rhizomelic chondrodysplasia punctata7 tests
  • Roberts syndrome6 tests
  • Salla disease8 tests
  • Sandhoff disease8 tests
  • Sanfilippo syndrome8 tests
  • Schimke immuno-osseous dysplasia6 tests
  • Severe combined immunodeficiency disease7 tests
  • Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency8 tests
  • Severe congenital neutropenia6 tests
  • Shprintzen-Goldberg syndrome4 tests
  • Sialidosis8 tests
  • Sickle cell disease and related diseases10 tests
  • Sitosterolemia4 tests
  • Sjögren-Larsson syndrome8 tests
  • Smith-Lemli-Opitz syndrome9 tests
  • Spinal muscular atrophy14 tests
  • Spinocerebellar ataxia type 108 tests
  • Spondylocostal dysostosis 2, autosomal recessive6 tests
  • Spongy degeneration of central nervous system10 tests
  • Stuve-Wiedemann syndrome6 tests
  • Sulfite oxidase deficiency6 tests
  • Supravalvar aortic stenosis4 tests
  • Tangier disease4 tests
  • Tay-Sachs disease11 tests
  • Trichohepatoenteric syndrome6 tests
  • Trimethylaminuria8 tests
  • Tyrosine hydroxylase deficiency6 tests
  • Tyrosinemia type I9 tests
  • Tyrosinemia type II6 tests
  • Tyrosinemia type III6 tests
  • Usher syndrome9 tests
  • Usher syndrome type 2C1 test
  • Usher syndrome type 3A1 test
  • Vanishing white matter disease6 tests
  • Velocardiofacial syndrome4 tests
  • Very long chain acyl-CoA dehydrogenase deficiency9 tests
  • Vitamin D-dependent rickets8 tests
  • Walker-Warburg congenital muscular dystrophy8 tests
  • Werner syndrome6 tests
  • Wilson disease10 tests
  • Wiskott-Aldrich syndrome6 tests
  • Wolff-Parkinson-White pattern5 tests
  • X-linked agammaglobulinemia6 tests
  • X-linked severe combined immunodeficiency7 tests
  • Xeroderma pigmentosum9 tests
  • Zellweger spectrum disorders8 tests

List of services

  • This lab has no services.

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 22D0650245, Expiration date: 2025-02-27
  • CAP, Number: 3397701, Expiration date: 2025-11-12
  • ISO15189, Number: 3397701, Expiration date: 2025-09-12

Licenses

  • CA - California Department of Public Health CDPH, Number: CDS 800051, Expiration date: 2024-12-07
  • MA - Executive Office of Health and Human Services EOHHS, Number: 5759, Expiration date: 2025-09-07
  • MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 591, Effective date: 2019-06-30 Non-expiring
  • NY - New York State Department of Health NYSDOH, Number: 4165, Expiration date: 2024-06-30
  • PA - Pennsylvania Department of Health PADOH, Number: 022051A, Expiration date: 2024-08-15
  • RI - State of Rhode Island Department of Health RIDOH, Number: LCO00631, Expiration date: 2025-12-30

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