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Genetic Labs

Houston, Texas

Genetic Laboratory
Medical Genetics Laboratories
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Medical Genetics Test Services

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  Fabry Disease OMIM GeneReview
  Factor V Leiden OMIM GeneReview
  FAM161A-Related Retinitis Pigmentosa OMIM
  FAM20C Related Disorders OMIM
  Familial Dysautonomia OMIM GeneReview
  Familial Exudative Vitreoretinopathy (4 gene panel by NGS) GeneReview
  Familial Hypercholesterolemia OMIM
  Familial Thrombocytopenia with Propensity to Acute Myelogenous Leukemia OMIM
  Fanconi-Bickel syndrome (SLC2A2) OMIM
  FARS2 Related disorders OMIM
  FASTKD2 - Related Disorders OMIM
  Fatty Acid Oxidation Deficiency (22 gene panel by NGS)
  FBN1 Related Disorders OMIM
  FBN2 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  FH - Related Disorders OMIM
  FISH Analysis - 1p36 Deletion Syndrome OMIM GeneReview
  FISH Analysis - Adrenal Hypoplasia Congenita OMIM GeneReview
  FISH Analysis - Alagille Syndrome, JAG1 Related OMIM GeneReview
  FISH Analysis - Angelman Syndrome Panel OMIM GeneReview
  FISH Analysis - Beckwith-Wiedemann Syndrome OMIM GeneReview
  FISH Analysis - Charcot-Marie-Tooth Neuropathy Type 1A OMIM GeneReview
  FISH Analysis - Cri-Du-Chat Syndrome OMIM
  FISH Analysis - DiGeorge/Velocardiofacial Syndrome Panel (22q and 10p) OMIM
  FISH Analysis - DiGeorge/Velocardiofacial Syndrome Type I (22q) OMIM GeneReview
  FISH Analysis - Glycerol Kinase Deficiency OMIM
  FISH Analysis - Hereditary Neuropathy with Liability to Pressure Palsies OMIM GeneReview
  FISH Analysis - Kallmann Syndrome Type I OMIM GeneReview
  FISH Analysis - Langer-Giedion Syndrome Panel (EXT1 and TRPS1) OMIM
  FISH Analysis - LIS1-Associated Lissencephaly/Subcortical Band Heterotopia OMIM GeneReview
  FISH Analysis - Microphthalmia with Linear Skin Defects Syndrome (MLS/MIDAS) OMIM GeneReview
  FISH Analysis - Miller-Dieker Syndrome OMIM GeneReview
  FISH Analysis - Multiple Exostoses Panel (EXT1 and EXT2) OMIM GeneReview
  FISH Analysis - Multiple Exostoses Type I (EXT1)   OMIM GeneReview
  FISH Analysis - Multiple Exostoses Type II/Potocki-Shaffer Panel (EXT2 and ALX4) OMIM GeneReview
  FISH Analysis - Neurofibromatosis Type I OMIM GeneReview
  FISH Analysis - Prader-Willi Syndrome Panel OMIM GeneReview
  FISH Analysis - Prenatal Aneuploidy
  FISH Analysis - Rubinstein-Taybi Syndrome - CREBBP Related OMIM GeneReview
  FISH Analysis - Sotos Syndrome OMIM GeneReview
  FISH Analysis - SRY Related Phenotypes OMIM GeneReview
  FISH Analysis - Trichorhinophalangeal Syndrome Type I OMIM
  FISH Analysis - WAGR Panel (WT1 and PAX6) OMIM GeneReview
  FISH Analysis - Williams Syndrome OMIM GeneReview
  FISH Analysis - Wilms Tumor (WT1) OMIM GeneReview
  FISH Analysis - Wolf-Hirschhorn Syndrome OMIM GeneReview
  FKBP10-Related Osteogenesis Imperfecta OMIM
  FLT3 Mutation Analysis OMIM
  FMR1 - Related Disorders OMIM GeneReview
  Focal Dermal Hypoplasia OMIM GeneReview
  FOXF1 - Related Disorders OMIM
  Friedreich Ataxia (FRDA) OMIM GeneReview
  Fructose 1,6 Bisphosphatase Deficiency (FBP1) OMIM
  FSCN2-Related Retinitis Pigmentosa OMIM
  FZD4 Related Disorders OMIM