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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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  C10orf2 (TWINKLE) - Related Disorders OMIM
  C2orf71-Related Retinitis Pigmentosa OMIM
  C8orf37-Related Retinitis Pigmentosa OMIM
  CA4-Related Retinitis Pigmentosa OMIM
  CALR Exon 9 Mutation Analysis
  Camurati-Engelmann Disease (TGFB1) OMIM
  Canavan Disease 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 (SLC22A5 (OCTN2)) OMIM
  Carnitine Determination - Plasma OMIM
  Carnitine Palmitoyltransferase IA Deficiency (CPT1A ) OMIM GeneReview
  Carnitine Palmitoyltransferase II Deficiency (CPT2) OMIM GeneReview
  CASP8 Related Disorders OMIM
  CAV3 Related Disorders OMIM
  CD247 Related Disorders (CD247) OMIM
  CD8 Deficiency, Familial (CD8A) OMIM
  CDC73 Related Disorders OMIM
  CDH1 Related Disorders OMIM
  CDH23 - Related Disorders OMIM
  CDKL5 - Related Disorders OMIM
  CDKN1C Related Disorders OMIM
  CDKN2A Related Disorders OMIM
  CEBPA Mutation Analysis - Germline - Blood
  CEBPA Mutation Analysis - Tumor
  Centronuclear Myopathy OMIM
  Centronuclear Myopathy 3 OMIM
  Centronuclear Myopathy 4 OMIM
  CEP290-Related Retinitis Pigmentosa OMIM
  Cerebrotendinous Xanthomatosis 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
  Chediak-Higashi Syndrome (LYST) OMIM
  CHEK2 Related Disorders OMIM
  Cholestasis Panel by NGS (7 gene panel by NGS)
  Chondrodysplasia punctata, rhizomelic, type 2 (GNPAT) OMIM
  CHRNA1 Related Disorders OMIM
  CHRNA7 - Related Disorders OMIM
  CHRNB1 Related Disorders OMIM
  CHRND Related Disorders OMIM
  CHRNE Related Disorders OMIM
  Chromosomal Microarray Analysis - CytoScan HD SNP Array
  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 - CVS
  Chromosome Analysis - Tissue
  Citrin Deficiency (SLC25A13) OMIM GeneReview
  Citrullinemia Type I OMIM GeneReview
  CLCN7-Related Osteopetrosis OMIM
  Cleidocranial Dysplasia OMIM GeneReview
  CLN6 Related Disorders OMIM
  CLN8 Related Disorders OMIM
  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 (20 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 Deficiency 6 OMIM
  Coenzyme Q10 Determination - Muscle OMIM
  COG6 Related Disorders (COG6) OMIM
  COL1A1 Related Disorders OMIM
  COL1A1/2 Related Disorders (2 gene panel by NGS)
  COL1A2 Related Disorders OMIM
  COL2A1 - Related Disorders OMIM GeneReview
  COL6A1 Related Disorders OMIM
  COL6A2 Related Disorders OMIM
  COL6A3 Related Disorders OMIM
  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
  Combined Pituitary Hormone Deficiency 2 OMIM
  Comprehensive Autism Panel - Female Specific
  Comprehensive Autism Panel - Male Specific
  Comprehensive B-Cell Clonality Analysis
  Comprehensive Hereditary Cancer Panel (61 gene panel by NGS)
  Comprehensive T-Cell Clonality Analysis
  Compton-North Congenital Myopathy OMIM
  Cone-rod Dystrophy 15 (CDHR1) OMIM
  Congenital & Distal Myopathy (39 gene panel by NGS)
  Congenital Disorder of Glycosylation Type Iu OMIM
  Congenital Disorder of Glycosylation, Type Ic (ALG6) OMIM
  Congenital Disorder of Glycosylation, Type Id (ALG3) OMIM
  Congenital Disorder of Glycosylation, Type If OMIM
  Congenital Disorder of Glycosylation, Type Ig (ALG12) OMIM
  Congenital Disorder of Glycosylation, Type Ih (ALG8) OMIM
  Congenital Disorder of Glycosylation, Type IIb OMIM
  Congenital Disorder of Glycosylation, Type IIc OMIM
  Congenital Disorder of Glycosylation, Type IId (B4GALT1) OMIM
  Congenital Disorder of Glycosylation, Type IIe OMIM
  Congenital Disorder of Glycosylation, Type IIf OMIM
  Congenital Disorder of Glycosylation, Type IIg OMIM
  Congenital Disorder of Glycosylation, Type IIh 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 Il (ALG9) 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 Disorder of Glycosylation, Type Iv (NGLY1) OMIM
  Congenital Disorders of Glycosylation - CDG Panel (36 gene panel by NGS) 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 Generalized Lipodystrophy Type 4 OMIM
  Congenital Hypothyroidism, IYD-Related OMIM
  Congenital Ichthyosis Autosomal Recessive 1 OMIM
  Congenital Muscular Dystrophy (25 gene panel by NGS)
  Congenital Muscular Dystrophy due to ITGA7 Deficiency OMIM
  Congenital Muscular Dystrophy Megaconial Type OMIM
  Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A 10 OMIM
  Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A 11 OMIM
  Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A 12 OMIM
  Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A 7 OMIM
  Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A 8 OMIM
  Congenital Myasthenia with Tubular Aggregates 1 OMIM
  Congenital Myasthenic Syndrome (17 gene panel by NGS)
  Congenital Myasthenic Syndrome Associated with Acetylcholine Receptor Deficiency (MUSK) OMIM
  Congenital Myasthenic Syndrome with Pre- and Postsynaptic Defects OMIM
  Congenital Myasthenic Syndrome, ALG14 Related OMIM
  Congenital Myopathy OMIM
  Congenital Myopathy (24 gene panel by NGS)
  Congential Myasthenic Syndrome Associated with Episodic Apnea 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
  CP Related Disorders 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
  CRYAB Related Disorders OMIM
  CTNS Related Disorders OMIM
  Custom Family Sequence Analysis
  Custom Proband Sequence Analysis
  Cutaneous Malignant Melanoma 3 (CDK4) OMIM
  CYP1B1 Related Disorders OMIM
  Cytochrome P450 2C19 (CYP2C19) Genotyping OMIM
  Cytochrome P450 2D6 (CYP2D6) Genotyping OMIM