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Genetic Labs

Houston, Texas

Genetic Laboratory
Medical Genetics Laboratories
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Medical Genetics Test Services

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  MAK-Related Retinitis Pigmentosa OMIM
  Malabsorptive Congenital Diarrhea 4 (NEUROG3) OMIM
  Maple Syrup Urine Disease (4 gene panel by NGS) GeneReview
  Maple Syrup Urine Disease Type 1A (BCKDHA) OMIM
  Maple Syrup Urine Disease Type 1B (BCKDHB) OMIM
  Maple Syrup Urine Disease Type 2 (DBT) OMIM GeneReview
  Maple Syrup Urine Disease Type 3 (DLD) OMIM
  MARS2 Related Disorders OMIM
  Maturity-Onset Diabetes of the Young (MODY) (25 gene panel by NGS)
  Maturity-onset Diabetes of the Young 6 (NEUROD1) OMIM
  Maturity-onset Diabetes of the Young, Type 11 (BLK) OMIM
  Maturity-onset Diabetes of the Young, Type VII (KLF11) OMIM
  MAX-Related Disorders
  MCAD Deficiency (ACADM) OMIM GeneReview
  MECP2 - Related Disorders OMIM GeneReview
  MEF2C - Related Disorders OMIM
  Menkes Disease (ATP7A) OMIM GeneReview
  MERTK-Related Retinitis Pigmentosa OMIM
  MET Related Disorders OMIM
  Methylcobalamin Deficiency, cblG Type (MTR) OMIM
  Methylmalonic Acid - Plasma GeneReview
  Methylmalonic Acidemia - 3 Gene Panel (MUT, MMAA, MMAB)
  Methylmalonic Acidemia - MCEE Related OMIM GeneReview
  Methylmalonic Acidemia - MMAA Related (cblA) OMIM GeneReview
  Methylmalonic Acidemia - MMAB Related (cblB) OMIM GeneReview
  Methylmalonic Acidemia - MMADHC Related OMIM GeneReview
  Methylmalonic Acidemia - MUT Related OMIM GeneReview
  Methylmalonic Acidemia and Homocysteinemia, cblX Type (HCFC1) OMIM
  Methylmalonic Aciduria and Homocystinuria, cblJ Type (ABCD4) OMIM
  Methylmalonic Aciduria due to Transcobalamin Receptor Defect (CD320) OMIM
  MHC Class II Deficiency Complementation Group B (RFXANK) OMIM
  Microcephaly, Epilepsy, and Diabetes Syndrome (IER3IP1) OMIM
  Microphthalmia, Isolated 5 Disorder (MFRP) OMIM
  Microsatellite Instability Analysis (NCI Panel) OMIM GeneReview
  Mismatch Repair Proteins Immunohistochemistry
  Mitchell-Riley Syndrome (RFX6) OMIM
  Mitochondrial Complex I Deficiency-FOXRED1 Related OMIM
  Mitochondrial Complex I Deficiency-NDUFA11 Related OMIM
  Mitochondrial Complex I Deficiency-NDUFA8 Related OMIM
  Mitochondrial Complex I Deficiency-NDUFAF3 Related OMIM
  Mitochondrial Complex I Deficiency-NDUFAF5 Related OMIM
  Mitochondrial Complex I Deficiency-NDUFB6 Related OMIM
  Mitochondrial Complex I Deficiency-NDUFV3 Related OMIM
  Mitochondrial Complex I Deficiency-NUBPL Related OMIM
  Mitochondrial Complex II Deficiency, SDHAF1 Related OMIM
  Mitochondrial Complex III Deficiency-TTC19 Related OMIM
  Mitochondrial Complex III Deficiency-UQCRB Related OMIM
  Mitochondrial Complex III Deficiency-UQCRQ Related OMIM
  Mitochondrial Complex IV Deficiency-COX4I1 Related OMIM
  Mitochondrial Complex IV Deficiency-COX4I2 Related OMIM
  Mitochondrial Complex IV Deficiency-COX7A1 Related OMIM
  Mitochondrial Complex IV Deficiency-TACO1 Related OMIM
  Mitochondrial Complex V Deficiency-ATP5E Related OMIM
  Mitochondrial Complex V Deficiency-ATPAF2 Related (ATP12) OMIM
  Mitochondrial Depletion Syndrome Panel by NGS (19 gene panel by NGS)
  Mitochondrial DNA Content (qPCR) Analysis - Liver
  Mitochondrial DNA Content (qPCR) Analysis - Skeletal Muscle
  Mitochondrial DNA Depletion Syndrome 11 (MGME1) OMIM
  Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) (FBXL4) OMIM
  Mitochondrial DNA Depletion Syndrome SUCLG2-Related OMIM
  Mitochondrial DNA Point Mutations and Deletions-NGS
  Mitochondrial Myopathy and Sideroblastic Anemia Type 1 (PUS1) OMIM
  Mitochondrial Myopathy and Sideroblastic Anemia Type 2 (YARS2)
  Mitochondrial Nonsyndromic Hearing Loss and Deafness Mutation Panel OMIM GeneReview
  Mitochondrial Phosphate Carrier Deficiency (SLC25A3, PHC) OMIM
  Mitochondrial Respiratory Chain Complex I Deficiency (25 nuclear gene panel by NGS) OMIM
  Mitochondrial Respiratory Chain Complex II Deficiency (6 nuclear gene panel OMIM
  Mitochondrial Respiratory Chain Complex III Deficiency (4 nuclear gene panel by NGS) OMIM
  Mitochondrial Respiratory Chain Complex IV Deficiency (12 nuclear gene panel by NGS) OMIM
  Mitochondrial Respiratory Chain Complex I-V Deficiency (50 nuclear gene pan
  Mitochondrial Respiratory Chain Complex V Deficiency (3 nuclear gene panel by NGS)
  Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skeletal Muscle OMIM GeneReview
  Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skin Fibroblasts OMIM GeneReview
  Mitochondrial/Metabolic (MitoMetŪPlus) Microarray Analysis
  Mitochondrial/Metabolic (MitoMetŪPlus) Microarray Analysis
  Mitome200-Dual Genome Panel by NGS (201 gene panel by NGS)
  Mitome200-Nuclear Gene Panel by NGS (164 gene panel by NGS)
  MKKS Related Disorders OMIM
  MKS1 Related Disorders OMIM
  MLH1 Immunohistochemistry
  MMACHC (cblC) - Related Disorders OMIM GeneReview
  MNGIE Syndrome (TYMP or ECGF1) OMIM GeneReview
  Modifier of Bardet-Biedl syndrome (CCDC28B) OMIM
  MODY Type I (HNF4A) OMIM
  Molybdenum Cofactor Deficiency - MOCS1 Related OMIM
  Molybdenum Cofactor Deficiency - MOCS2 Related OMIM
  MPD Panel - JAK2V617F, JAK2 Exon 12, MPL Exon 10
  MPL Exon 10 Mutation Analysis OMIM
  MPV17 - Related Disorders OMIM
  MRPL40 Related disorders OMIM
  MRPL44 Related disorders OMIM
  MRPS18A Related disorders OMIM
  MRPS2 Related disorders OMIM
  MRRF Related disorders OMIM
  MSH2 Immunohistochemistry
  MSH6 Immunohistochemistry
  MTFMT Related disorders OMIM
  MTHFR Thermolabile Variant Analysis OMIM
  MTRR Related Disorders OMIM GeneReview
  Mucolipidosis I [Sialidosis] OMIM
  Mucopolysaccharidosis Type I OMIM GeneReview
  Mucopolysaccharidosis Type II OMIM GeneReview
  Mucopolysaccharidosis Type IVA OMIM
  Mucopolysaccharidosis Type VI (ARSB) OMIM
  Multiple Acyl-CoA Dehydrogenase Deficiency - ETFA Related OMIM
  Multiple Acyl-CoA Dehydrogenase Deficiency - ETFB Related OMIM
  Multiple Acyl-CoA Dehydrogenase Deficiency - ETFDH Related OMIM
  Multiple Acyl-CoA Dehydrogenase Deficiency Panel (ETFA, ETFB & ETFDH)
  Multiple Endocrine Neoplasia Type 1 OMIM GeneReview
  Multiple Intestinal Atresia (TTC7A) OMIM
  MUTYH (MYH) - Associated Polyposis OMIM
  MYH11 Mutation AnalysisJohn Welsh Cardiovascular Diagnostic Laboratory
  MYLK Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  MYO7A - Related Disorders OMIM
  Myopathy with Deficiency of ISCU OMIM GeneReview
  Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay (GFER) OMIM
  Myopathy/Rhabdomyolysis Panel by NGS (27 gene panel by NGS)
  Myotonic Dystrophy Type 1 OMIM GeneReview