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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor 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
   Familial Exudative Vitreoretinopathy (4 gene panel by NGS) GeneReview
   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
   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
   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
   FLCN 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