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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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   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
   SCN4A Related Disorders OMIM
   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
   Segawa Syndrome Recessive OMIM
   Selective T-cell Defect (ZAP70) OMIM
   SEMA4A-Related Retinitis Pigmentosa OMIM
   SEPN1 Related Disorders OMIM
   Sequential Trio Whole Exome Sequencing
   SERPINA1 Related Disorders (SERPINA1) OMIM
   Severe Combined Immunodeficiency (9 gene panel by NGS)
   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
   SGCD Related Disorders OMIM
   Shwachman-Bodian-Diamond Syndrome OMIM
   Sickle Cell Disease OMIM GeneReview
   Sjogren-Larsson Syndrome OMIM
   SLC16A1 Related Disorders OMIM
   SLC17A5 Related Disorders OMIM
   SLC25A4 (ANT1) - Related Disorders OMIM
   SLC26A2 Related Disorders OMIM
   SLC26A4 Related Disorders OMIM
   SLC9A3R1 Related Disorders OMIM
   SLC9A6 - Related Syndromic Mental Retardation OMIM
   SMAD4 Related Disorders OMIM
   Smith-Lemli-Opitz Syndrome OMIM GeneReview
   Smith-Magenis Syndrome OMIM GeneReview
   SMPD1 Related Disorders OMIM
   SNRNP200-Related Retinitis Pigmentosa OMIM
   SOST-Related Sclerosing Bone Dysplasias OMIM
   SP7-Related Osteogenesis Imperfecta OMIM
   Spastic Ataxia Charlevoix-Saguenay Type 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
   SYNE1 Related Disorders OMIM