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Results: 21 to 40 of 50

Tests names and labsConditionsGenes, analytes, and microbesMethods

Kallmann syndrome panel. 9-gene NGS panel.

Genologica Medica
Spain
179
  • C Sequence analysis of the entire coding region

Holoprosencephaly panel. 12-gene NGS panel.

Genologica Medica
Spain
2712
  • C Sequence analysis of the entire coding region

Genital Abnormalities / Sex Development Disorders Panel

Genologica Medica
Spain
9549
  • C Sequence analysis of the entire coding region

Kallmann Syndrome Genetic Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
2524
  • C Sequence analysis of the entire coding region

Kallmann Syndrome

Asper Biogene Asper Biogene LLC
Estonia
2725
  • C Sequence analysis of the entire coding region

Hypogonadotropic hypogonadism with or without anosmia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2424
  • C Sequence analysis of the entire coding region

Kallmann Syndrome & Hypogonadotropic Hypogonadism NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3439
  • C Sequence analysis of the entire coding region

Male Infertility NGS Panel

Fulgent Genetics
United States
7945
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Infertility NGS Panel

Fulgent Genetics
United States
9256
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Female Infertility NGS Panel

Fulgent Genetics
United States
7641
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nonsyndromic disorders of sexual development: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1712
  • C Sequence analysis of the entire coding region

Septo-Optic Dysplasia , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
119
  • C Sequence analysis of the entire coding region

Kallmann Syndrome , Panel Massive Sequencing (NGS) 20 Genes

Reference Laboratory Genetics
Spain
2120
  • C Sequence analysis of the entire coding region

Holoprosencephaly, Panel Massive Sequencing (NGS) 8 Genes

Reference Laboratory Genetics
Spain
88
  • C Sequence analysis of the entire coding region

KALLMANN SYNDROME

Laboratorio de Genetica Clinica SL
Spain
66
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGF8 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KALLLMAN SYNDROME (HYPOGONADOTROPIC HYPOGONADISM)

Laboratorio de Genetica Clinica SL
Spain
66
  • C Sequence analysis of the entire coding region

Kallmann Syndrome Type 6 , Sequencing FGF8 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Brain malformations

Asper Biogene Asper Biogene LLC
Estonia
318252
  • C Sequence analysis of the entire coding region

qGenEx Craniofacial Anomalies

Quantitative Genomic Medicine Laboratories, SL
Spain
135136
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 50

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.