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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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  SAG-Related Retinitis Pigmentosa OMIM
  SCAD Deficiency (ACADS) OMIM GeneReview
  Schmid Metaphyseal Chondrodysplasia OMIM
  SCID Newborn Screening Follow-up Panel
  SCID, Autosomal Recessive, T- Negative/B-Positive Type OMIM
  SCN4B Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  SCN5A Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  SCO1 - Related Disorders OMIM
  SCO2 - Related Disorders (SCO2 or SCO1L) OMIM
  SDHA - Related Disorders OMIM
  SDHAF2 - Related Disorders (SDH5) OMIM GeneReview
  SDHB - Related Disorders OMIM GeneReview
  SDHC - Related Disorders OMIM GeneReview
  SDHD - Related Disorders OMIM GeneReview
  SEMA4A-Related Retinitis Pigmentosa OMIM
  SERPINA1 Related Disorders (SERPINA1) OMIM
  Severe Combined Immunodeficiency (9 gene panel by NGS) GeneReview
  Severe Combined Immunodeficiency, Athabascan Type OMIM
  Severe Combined Immunodeficiency, B Cell-Negative OMIM
  Severe Combined Immunodeficiency, T-Cell Negative, B-Cell/Natural Killer Cell-Positive Type (IL7R) OMIM
  Sickle Cell Disease OMIM GeneReview
  SLC25A4 (ANT1) - Related Disorders OMIM
  SLC2A10 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  SLC9A3R1 Related Disorders OMIM
  SLC9A6 - Related Syndromic Mental Retardation OMIM
  SMAD3 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  SMAD4 Mutation AnalysisJohn Welsh Cardiovascular Diagnostic Laboratory
  SMAD8 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  Smith-Lemli-Opitz Syndrome OMIM GeneReview
  Smith-Magenis Syndrome OMIM GeneReview
  SNRNP200-Related Retinitis Pigmentosa OMIM
  SNTA1 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  SOST-Related Sclerosing Bone Dysplasias OMIM
  SP7-Related Osteogenesis Imperfecta OMIM
  SPATA7-Related Retinitis Pigmentosa OMIM
  Spinal Muscular Atrophy Diagnostic Test OMIM GeneReview
  Spinocerebellar Ataxia Type 1 OMIM GeneReview
  Spinocerebellar Ataxia Type 10 OMIM GeneReview
  Spinocerebellar Ataxia Type 14 (PRKCG) OMIM
  Spondylocheirodysplasia, Ehlers-Danlos Syndrome (SLC39A13) OMIM
  SRD5A3 Related Disorders OMIM
  SRY Molecular Analysis OMIM GeneReview
  Succinic Semialdehyde Dehydrogenase Deficiency (ALDH5A1) OMIM
  Succinyladenosine - CSF
  SUCLA2 - Related Disorders OMIM GeneReview
  SUCLG1 - Related Disorders OMIM
  Sulfocysteine Determination - Urine OMIM
  SURF1 - Related Disorders OMIM