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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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   ABCA4 - Related Disorders OMIM GeneReview
   ABCC8 Related Disorders OMIM
   Acetyl-CoA Carboxylase Deficiency (ACACA) OMIM
   Acetyl-CoA Carboxylase-Beta Deficiency (ACACB) OMIM
   Achondroplasia OMIM GeneReview
   Acid Sphingomyelinase Deficiency OMIM GeneReview
   ACTA1 Related Disorders OMIM
   Acute Lymphoblastic Leukaemia (PAX5) OMIM
   Acute Myeloid Leukemia (CEBPA) OMIM
   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
   Agenesis of the Corpus Callosum with Peripheral Neuropathy OMIM
   AIPL1-Related Retinitis Pigmentosa OMIM
   AKT2 Related Disorders OMIM
   Alagille Syndrome (JAG1) OMIM GeneReview
   Albinism (13 gene panel by NGS)
   ALK Gene Rearrangement by FISH Analysis OMIM
   Alpha-Mannosidosis Types I and II OMIM
   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
   Amish Type Nemaline Myopathy 5 OMIM
   Androgen Insensitivity Syndrome OMIM GeneReview
   Angelman Syndrome OMIM GeneReview
   ANKH Related Disorders OMIM
   ANO5 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
   ARL6 Related Disorders OMIM
   ARX - Related Disorders OMIM
   Arylsulfatase A Deficiency [Metachromatic Leukodystrophy] OMIM GeneReview
   Ashkenazic Genetic Disease Panel
   Aspartylglycosaminuria OMIM
   Aspartylglycosaminuria (AGA) OMIM
   Ataxia with Isolated Vitamin E Deficiency OMIM
   Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (APTX) OMIM
   Ataxia, Posterior Column, with Retinitis Pigmentosa (FLVCR1) OMIM
   Ataxia-Telangiectasia-like Disorder (MRE11A) OMIM
   ATM Related Disorders 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
   Autosomal Dominant Nemaline Myopathy 6 OMIM
   Autosomal Recessive Centronuclear Myopathy OMIM
   Autosomal Recessive Nemaline Myopathy 2 OMIM
   Autosomal Recessive Nemaline Myopathy 7 OMIM
   Autosomal Recessive Nemaline Myopathy 8 OMIM