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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