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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Miraca 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 Dysautonomia OMIM
  Familial Exudative Vitreoretinopathy (4 gene panel by NGS) GeneReview
  Familial Hemophagocytic Lymphohistiocytosis 3 (UNC13D) OMIM
  Familial Hemophagocytic Lymphohistiocytosis 4 (STX11) OMIM
  Familial Hemophagocytic Lymphohistiocytosis 5 (STXBP2) OMIM
  Familial Hypercholesterolemia OMIM
  Familial Thrombocytopenia with Propensity to Acute Myelogenous Leukemia OMIM
  Fanconi Anemia Complementation Group C OMIM
  Fanconi Anemia Complementation Group N (PALB2) OMIM
  Fanconi Anemia Complementation Group O (RAD51C) 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
  FH - Related Disorders OMIM
  FHL1 Related Disorders OMIM
  Fibrodysplasia Ossificans Progressiva 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
  FKRP Related Disorders OMIM
  FKTN Related Disorders OMIM
  FLCN Related Disorders OMIM
  FLNC Related Disorders 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