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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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  ABCA4 - Related Disorders OMIM GeneReview
  Acetyl-CoA Carboxylase Deficiency (ACACA) OMIM
  Acetyl-CoA Carboxylase-Beta Deficiency (ACACB) OMIM
  Achondroplasia OMIM GeneReview
  Acid Sphingomyelinase Deficiency OMIM GeneReview
  ACTA2 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  Acute Recurrent Myoglobinuria - LPIN1 Related OMIM
  Acylcarnitine Analysis - Plasma OMIM
  Acyl-CoA Dehydrogenase 9 Deficiency (ACAD9) OMIM
  Acyl-CoA Dehydrogenase, Short/Branched Chain Deficiency (ACADSB) OMIM
  Adenine Phosphoribosyltransferase Deficiency (APRT) OMIM
  Adenosine Deaminase Deficiency OMIM GeneReview
  Adenosine Deaminase Deficiency (ADA) OMIM
  Adenylosuccinase Deficiency (ADSL) OMIM
  Adrenoleukodystrophy (ABCD1) OMIM GeneReview
  Adult Screening Exome Sequencing
  AIPL1-Related Retinitis Pigmentosa OMIM
  AKAP9 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  AKT1 Mutation Analysis - Tumor OMIM
  Alagille Syndrome (JAG1) OMIM GeneReview
  Albinism (13 gene panel by NGS)
  ALK Gene Rearrangement by FISH Analysis OMIM
  ALK1 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  ALPL Related Disorders OMIM
  AMACR Related Disorders (AMACR) OMIM
  Amino Acid Analysis - Cerebrospinal Fluid
  Amino Acid Analysis - Plasma
  Amino Acid Analysis - Urine
  Amish Lethal Microcephaly (SLC25A19) OMIM GeneReview
  Androgen Insensitivity Syndrome OMIM GeneReview
  Angelman Syndrome OMIM GeneReview
  ANK2 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  ANKH Related Disorders OMIM
  APC - Associated Polyposis Conditions OMIM GeneReview
  Arginase Deficiency OMIM GeneReview
  Arginine: Glycine Amidinotransferase (GATM) Deficiency (AGAT) OMIM GeneReview
  Argininosuccinate Lyase Deficiency OMIM GeneReview
  ARX - Related Disorders OMIM
  Arylsulfatase A Deficiency [Metachromatic Leukodystrophy] OMIM GeneReview
  Ashkenazic Genetic Disease Panel
  Ashkenazic Genetic Disease Screen (with Cystic Fibrosis)
  Ashkenazic Genetic Disease Screen (without Cystic Fibrosis)
  Aspartylglycosaminuria OMIM
  Aspartylglycosaminuria (AGA) OMIM
  Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (APTX) OMIM
  Ataxia, Posterior Column, with Retinitis Pigmentosa (FLVCR1) OMIM
  ATP5A1 Related disorders OMIM
  ATP6V0A2 Related Disorders OMIM
  Autism Panel - Biochemistry 3-Plex
  Autism Panel - Biochemistry 5- Plex
  Autism Panel - Biochemistry 8-Plex
  Autoimmune Polyendocrinopathy 1 OMIM