GTR Home > Laboratories > Greenwood Genetic Center Diagnostic Laboratories

Greenwood Genetic Center Diagnostic Laboratories

GTR Lab ID: 1019
Last updated: 2013-05-13
Annual Review past due read more

General information

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Personnel

  • Director: Monica Basehore, PhD, ABMG, FACMG, Lab Director
    Phone: 864-388-1043
    Fax: 864-941-8141
    Email: mbasehore@ggc.org
  • Director: Michael Friez, PhD, ABMG, FACMG, Lab Director
  • Director: Julie Jones, PhD, ABMG, FACMG, Lab Director
    Phone: 864-388-1049
    Fax: 864-941-8141
    Email: juliejones@ggc.org
  • Kellie King, MS, CGC, Genetic Counselor
    Phone: 864-388-1055
    Fax: 864-941-8133
    Email: kking@ggc.org

Conditions and tests

  • Aarskog syndrome1 test
  • Achondroplasia2 tests
  • Acrocephalosyndactyly type I1 test
  • Adrenoleukodystrophy1 test
  • Allan-Herndon-Dudley syndrome1 test
  • Angelman syndrome1 test
  • Aspartylglycosaminuria1 test
  • ATR-X syndrome1 test
  • Atypical Rett syndrome1 test
  • Beta-D-mannosidosis1 test
  • Biotinidase deficiency1 test
  • Borjeson-Forssman-Lehmann syndrome1 test
  • Carbohydrate-deficient glycoprotein syndrome type I1 test
  • Cardio-facio-cutaneous syndrome1 test
  • Carnitine palmitoyltransferase II deficiency1 test
  • CHARGE association1 test
  • Christianson syndrome1 test
  • Citrullinemia type I1 test
  • Coffin-Lowry syndrome1 test
  • Combined deficiency of sialidase AND beta galactosidase1 test
  • Congenital disorder of glycosylation type 1B1 test
  • Congenital disorder of glycosylation type 1C1 test
  • Costello syndrome1 test
  • Craniosynostosis syndrome1 test
  • Creatine deficiency, X-linked1 test
  • Crouzon syndrome1 test
  • Crouzon syndrome with acanthosis nigricans1 test
  • Cutis Gyrata syndrome of Beare and Stevenson1 test
  • Cutis laxa, X-linked1 test
  • Deafness, autosomal dominant 3a1 test
  • Deafness, autosomal recessive 1A1 test
  • Deafness, nonsyndromic sensorineural, mitochondrial1 test
  • Deficiency of alpha-mannosidase1 test
  • Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase1 test
  • Disorder of organic acid metabolism1 test
  • Duchenne muscular dystrophy1 test
  • Early infantile epileptic encephalopathy 41 test
  • Epileptic encephalopathy, early infantile, 11 test
  • FG syndrome1 test
  • Fragile X syndrome1 test
  • FRAXE1 test
  • Fucosidosis1 test
  • Gaucher disease1 test
  • Glutaric aciduria, type 11 test
  • GM1 Gangliosidosis1 test
  • Greig cephalopolysyndactyly syndrome1 test
  • Hay-Wells syndrome of ectodermal dysplasia1 test
  • Hereditary hemochromatosis1 test
  • Hurler syndrome1 test
  • Hypochondroplasia2 tests
  • Jackson-Weiss syndrome1 test
  • Kabuki make-up syndrome1 test
  • Kallmann syndrome 51 test
  • L1 Syndrome1 test
  • LEOPARD syndrome1 test
  • Marfan's syndrome1 test
  • Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
  • Menkes kinky-hair syndrome1 test
  • Mucolipidosis III Gamma1 test
  • Mucopolysaccharidosis type VI1 test
  • Mucopolysaccharidosis, MPS-II1 test
  • Mucopolysaccharidosis, MPS-IV-A1 test
  • Mucopolysaccharidosis, MPS-IV-B1 test
  • Noonan syndrome 61 test
  • Noonan syndrome 71 test
  • Opitz-Frias syndrome1 test
  • Ornithine carbamoyltransferase deficiency1 test
  • Otopalatodigital Spectrum Disorders1 test
  • Pallister-Hall syndrome1 test
  • Pelizaeus-Merzbacher disease1 test
  • Pfeiffer syndrome1 test
  • Phenylketonuria1 test
  • Pitt-Hopkins syndrome1 test
  • Postaxial polydactyly type A11 test
  • Prader-Willi syndrome1 test
  • Progressive sclerosing poliodystrophy1 test
  • PTEN hamartoma tumor syndrome1 test
  • Renal carnitine transport defect1 test
  • Renpenning syndrome 11 test
  • Rett syndrome, congenital variant1 test
  • Rett's disorder1 test
  • Saethre-Chotzen syndrome1 test
  • Severe X-linked myotubular myopathy1 test
  • Sialidosis, type II1 test
  • Simpson-Golabi-Behmel syndrome1 test
  • Sotos' syndrome1 test
  • Steinert myotonic dystrophy syndrome1 test
  • Thanatophoric dysplasia type 11 test
  • Thanatophoric dysplasia, type 21 test
  • Thrombophilia1 test
  • Thrombophilia due to activated protein C resistance1 test
  • X-linked intellectual disability1 test
  • X-linked lissencephaly1 test
  • X-linked mental retardation with marfanoid habitus syndrome1 test
  • X-linked mental retardation, CASK-related1 test

List of services

  • Uniparental Disomy (UPD) Testing, comments
  • X-Chromosome Inactivation Studies

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 42D0689473, Expiration date: 2013-05-13
  • CAP, Number: 3833401, Expiration date: 2013-07-15

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