skip to content »

Genetic Labs

Houston, Texas

Genetic Laboratory
Medical Genetics Laboratories
not shown on screen

Medical Genetics Test Services

View Custom Req   |    Tests in Custom Req: 0
Search Tests: (Search by disease, test name, gene name, test code, or keyword. Return to test index.)

    Browse:  # A B C D E F G H I J K L M N O P Q R S T U V W X Y Z




  LAMP2 Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  LARS2-Related Disorders
  LCA5-Related Leber Congenital Amaurosis OMIM
  LCAD Deficiency (ACADL) OMIM
  Leber Congenital Amaurosis Panel (19 gene panel by NGS)
  Leber Congenital Amaurosis, Calcium Binding Protein 4 Deficiency (CABP4) OMIM GeneReview
  Leber Congenital Amaurosis, IQ Motif Containing B1 Deficiency (IQCB1) OMIM GeneReview
  Leber Congenital Amaurosis, Nicotinamide Nucleotide Adenylyltransferase 1 Deficiency (NMNAT1) OMIM GeneReview
  Leber Congenital Amaurosis, Orthodenticle Homeobox 2 Deficiency (OTX2) OMIM
  Leber Congenital Amaurosis, Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 Deficiency (KCNJ13) OMIM GeneReview
  Leigh Disease
  Leigh Disease (90 genel panel by NGS) GeneReview
  Leigh Syndrome (LRPPRC) OMIM
  Lesch-Nyhan Syndrome OMIM GeneReview
  Leukemia Mutation Panel
  Leukoencephalopathy (DARS2) OMIM GeneReview
  Leukoencephalopathy with dystonia and motor neuropathy (SCP2) OMIM
  Li-Fraumeni Syndrome OMIM GeneReview
  Liver Failure, Acute Infantile (TRMU) OMIM
  LMBRD1 (cblF)-Related Disorders OMIM GeneReview
  LMNA Mutation Analysis John Welsh Cardiovascular Diagnostic Laboratory
  Low Bone Mass Panel by NGS (23 gene panel by NGS)
  Lowe Syndrome OMIM GeneReview
  LRAT-Related Retinitis Pigmentosa OMIM
  LRP5 Related Disorders OMIM