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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
  Selective T-cell Defect (ZAP70) OMIM
  SEMA4A-Related Retinitis Pigmentosa OMIM
  SERPINA1 Related Disorders (SERPINA1) OMIM
  Severe Combined Immunodeficiency (9 gene panel by NGS) GeneReview
  Severe Combined Immunodeficiency (SCID) (46 gene panel by NGS)
  Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation (NHEJ1) OMIM
  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 (PTPRC) OMIM
  Severe Combined Immunodeficiency, T-Cell Negative, B-Cell/Natural Killer Cell-Positive Type (IL7R) OMIM
  Shwachman-Bodian-Diamond syndrome (SBDS) OMIM
  Sickle Cell Disease OMIM GeneReview
  SLC16A1 Related Disorders OMIM
  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
  SMAD4 Related Disorders OMIM
  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
  Spastic Paraplegia 7, Autosomal Recessive (SPG7) 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
  STAT5B Related Disorders OMIM
  STIM1 Related Disorders OMIM
  STK11 Related Disorders OMIM
  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