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Genetic Labs

Houston, Texas

Genetic Laboratory
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Medical Genetics Test Services

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  C10orf2 (TWINKLE) - Related Disorders OMIM
  C2orf71-Related Retinitis Pigmentosa OMIM
  C8orf37-Related Retinitis Pigmentosa OMIM
  CA4-Related Retinitis Pigmentosa OMIM
  CACNA1B Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  CACNA1C Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  CALR Exon 9 Mutation Analysis
  Camurati-Engelmann Disease (TGFB1) OMIM
  Canavan Disease Ashkenazic Mutation Panel OMIM GeneReview
  Cancer Chromosomal Microarray Analysis - 180K CGH/SNP Array
  Cancer Chromosomal Microarray Analysis - BCM 400K CGH/SNP Array
  Cancer Chromosomal Microarray Analysis - CytoScan HD SNP Array - Tumor
  Cancer Exome Sequencing
  Cancer Gene Mutation Panel Version 2
  Carbamoyl Phosphate Synthetase Deficiency OMIM GeneReview
  Carbamoyl Phosphate Synthetase Deficiency (CPS1) OMIM GeneReview
  Cardiofaciocutaneous Syndrome - MAP2K1 Related OMIM GeneReview
  Cardiofaciocutaneous Syndrome - MAP2K2 Related OMIM GeneReview
  Carnitine Acylcarnitine Translocase (CACT) Deficiency (SLC25A20 ) OMIM
  Carnitine Biosynthesis Panel - Plasma OMIM
  Carnitine Biosynthesis Panel - Urine OMIM
  Carnitine Deficiency, Systemic OMIM
  Carnitine Determination - Plasma OMIM
  Carnitine Palmitoyltransferase IA Deficiency (CPT1A ) OMIM GeneReview
  Carnitine Palmitoyltransferase II Deficiency (CPT2) OMIM GeneReview
  CASQ2 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  CAV3 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  CDH23 - Related Disorders OMIM
  CDKL5 - Related Disorders OMIM
  CEBPA Mutation Analysis - Germline - Blood
  CEBPA Mutation Analysis - Tumor - FFPE
  CEBPA Mutation Analysis - Tumor - Non-FFPE
  CEP290-Related Retinitis Pigmentosa OMIM
  CERKL-Related Retinitis Pigmentosa OMIM
  CFTR - 5T Variant Analysis OMIM GeneReview
  CFTR Sequence Analysis OMIM GeneReview
  CFTR-Related Disorders Mutation Panel OMIM GeneReview
  CHD7 - Related Disorders OMIM
  Cholestasis Panel by NGS
  Chondrodysplasia punctata, rhizomelic, type 2 (GNPAT) OMIM
  CHRNA7 - Related Disorders OMIM
  Chromosomal Microarray Analysis - CytoScan HD SNP Array - Non-Tumor
  Chromosomal Microarray Analysis - HR
  Chromosomal Microarray Analysis - HR + SNP Screen (Comprehensive)
  Chromosomal Microarray Analysis - POC (for paraffin-embedded tissue only)
  Chromosome Analysis - Blood
  Chromosome Analysis - Prenatal - Amniotic Fluid
  Chromosome Analysis - Prenatal - Amniotic Fluid with ACHE
  Chromosome Analysis - Prenatal - Amniotic Fluid with AFP
  Chromosome Analysis - Prenatal - Amniotic Fluid with AFP and ACHE
  Chromosome Analysis - Prenatal - Amniotic Fluid with AFP, ACHE, and FH
  Chromosome Analysis - Prenatal - CVS
  Chromosome Analysis - Tissue
  Citrin Deficiency (SLC25A13) OMIM GeneReview
  Citrullinemia Type I OMIM GeneReview
  CLCN7-Related Osteopetrosis OMIM
  Cleidocranial Dysplasia OMIM GeneReview
  CMA-Expanded and Limited Karyotype - Prenatal - Amniotic Fluid
  CMA-Expanded and Limited Karyotype - Prenatal - CVS
  CMA-Targeted and Limited Karyotype - Prenatal - Amniotic Fluid
  CMA-Targeted and Limited Karyotype - Prenatal - CVS
  CNGA1-Related Retinitis Pigmentosa OMIM
  CNGB1-Related Retinitis Pigmentosa OMIM
  Cobalamin Metabolism Panel (9 gene panel by NGS)
  Coenzyme Q10 Deficiency - CABC1 (ADCK3) Related OMIM
  Coenzyme Q10 Deficiency - COQ2 Related (COQ2, CL640, FLJ26072) OMIM
  Coenzyme Q10 Deficiency - COQ9 Related OMIM
  Coenzyme Q10 Deficiency - PDSS1 Related (PDSS1, COQ1, TPT) OMIM
  Coenzyme Q10 Deficiency - PDSS2 Related (PDSS2, bA59I9.3) OMIM
  Coenzyme Q10 Determination - Muscle OMIM
  COG6 Related Disorders (COG6) OMIM
  COL1A1/2 Related Disorders, Low Bone Mass, Osteogenesis Imperfecta, Ehlers-Danlos Syndrome, Caffey Disease (2 gene panel by NGS)
  COL1A2 Related Disorders OMIM
  COL2A1 - Related Disorders OMIM GeneReview
  Combined Malonic & Methylmalonic Aciduria (ACSF3) OMIM
  Combined Oxidative Phosphorylation Deficiency - MRPS16 Related OMIM
  Combined Oxidative Phosphorylation Deficiency - TSFM Related (EF-TS, EF-Tsmt) OMIM
  Combined Oxidative Phosphorylation Deficiency - TUFM Related OMIM
  Combined Oxidative Phosphorylation Deficiency 1 (GFM1) OMIM
  Combined Oxidative Phosphorylation Deficiency 5 (MRPS22) OMIM
  Combined Oxidative Phosphorylation Deficiency 7 (C12orf65) OMIM
  Combined Oxidative Phosphorylation Deficiency 8 (AARS2) OMIM
  Complex IV (COX) Deficiency Panel - Nuclear Genes (SURF1, SCO1, SCO2, COX10) OMIM
  Comprehensive Autism Panel - Female Specific
  Comprehensive Autism Panel - Male Specific
  Comprehensive B-Cell Clonality Analysis
  Comprehensive B-Cell Clonality Analysis - FFPE
  Comprehensive Hereditary Cancer Panel
  Comprehensive mtDNA Analysis by NGS
  Comprehensive T-Cell Clonality Analysis
  Comprehensive T-Cell Clonality Analysis - FFPE
  Cone-rod Dystrophy 15 (CDHR1) OMIM
  Congenital disorder of glycosylation, type IIi (COG5) OMIM
  Congenital disorder of glycosylation, type IIj (COG4) OMIM
  Congenital disorder of glycosylation, type IIk (TMEM165) OMIM
  Congenital disorder of glycosylation, type IIm (SLC35A2) OMIM
  Congenital disorder of glycosylation, type Ip (ALG11) OMIM
  Congenital disorder of glycosylation, type Ir (DDOST) OMIM
  Congenital disorder of glycosylation, type Is (ALG13) OMIM
  Congenital Disorders of Glycosylation - CDG Panel (27 gene panel by NGS) OMIM GeneReview
  Congenital Disorders of Glycosylation (TUSC3) OMIM
  Congenital Disorders of Glycosylation MPI Related OMIM GeneReview
  Congenital Disorders of Glycosylation PMM2 Related OMIM GeneReview
  Congenital Disorders of Glycosylation Type Ie (DPM1) OMIM
  Congenital Disorders of Glycosylation Type Ii OMIM GeneReview
  Congenital Disorders of Glycosylation Type IIa (MGAT2) OMIM
  Congenital Disorders of Glycosylation Type Ik OMIM GeneReview
  Congenital Disorders of Glycosylation Type Im (DOLK) OMIM GeneReview
  Congenital Disorders of Glycosylation Type In (RFT1) OMIM
  Congenital Disorders of Glycosylation Type Io (DPM3) OMIM
  Congenital Hypothyroidism, IYD-Related OMIM
  CoQ10 Deficiency (5 gene panel by NGS) OMIM
  Coronary Heart Disease Risk Factor (9p21 rs10757278)
  Costello Syndrome - HRAS Related OMIM GeneReview
  COX10 - Related Disorders OMIM
  COX15 - Related Disorders OMIM
  COX6B1 - Related Disorders (COXG) OMIM
  CPT1B - Related Disorders OMIM
  CRB1-Related Retinitis Pigmentosa OMIM
  Creatine and Guanidinoacetate Determination - Plasma OMIM GeneReview
  Creatine and Guanidinoacetate Determination - Urine OMIM GeneReview
  Creatine Panel
  Creatine Transporter Deficiency - SLC6A8 Related OMIM GeneReview
  CRX-Related Retinitis Pigmentosa OMIM
  Custom Family Sequence Analysis
  Custom Proband Sequence Analysis
  Cytochrome P450 2C19 (CYP2C19) Genotyping OMIM
  Cytochrome P450 2D6 (CYP2D6) Genotyping OMIM