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Results: 1 to 20 of 160

Tests names and labsConditionsGenes, analytes, and microbesMethods

Smith-Lemli-Opitz syndrome, 270400, Autosomal recessive; SLOS (Smith-Lemli-Opitz syndrome) (DHCR7 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz syndrome, 270400, Autosomal recessive; SLOS (Smith-Lemli-Opitz syndrome) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Smith-Lemli-Opitz syndrome, 270400, Autosomal recessive; SLOS (Smith-Lemli-Opitz syndrome) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Smith-Lemli-Opitz syndrome, 270400, Autosomal recessive; SLOS (Smith-Lemli-Opitz syndrome) (DHCR7 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome

Myriad Genetics, Inc.
United States
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz syndrome

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz syndrome

Center for Human Genetics, Inc
United States
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome

Asper Biogene Asper Biogene LLC
Estonia
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • A Analyte
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

SMITH-LEMLI-OPITZ SYNDROME

Laboratorio de Genetica Clinica SL
Spain
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome

Laboratory of Human Genetics GENOMED Health Care Center
Poland
11
  • E Sequence analysis of select exons

Smith-Lemli-Opitz syndrome

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

DHCR7 Gene Smith-Lemli-Opitz syndrome NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

DHCR7 - Smith-Lemli-Opitz syndrome

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome via the DHCR7 Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Smith-Lemli-Opitz Syndrome (DHCR7 Single Gene Test)

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome, DHCR7 sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Smith-Lemli-Opitz Syndrome (deficiency of 7-dehydrocholesterol reductase, sequence analysis of DHCR7 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 160

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.