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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 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
   Critical Trio Whole Exome Sequencing
   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