Clinical and research tests for 613986 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 43

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Septo-optic dysplasia panel. Panel NGS genes: HESX1, OTX2, PAX6, SOX2. Genologica Medica Spain	11	4	C Sequence analysis of the entire coding region
Combined Pituitary Hormone Deficiency Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	12	10	C Sequence analysis of the entire coding region
Comprehensive Short Stature Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	82	60	C Sequence analysis of the entire coding region
Growth Hormone Deficiency Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	15	11	C Sequence analysis of the entire coding region
Female Infertility Asper Biogene Asper Biogene LLC Estonia	85	64	C Sequence analysis of the entire coding region
Pituitary hormone deficiency, combined: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	8	6	C Sequence analysis of the entire coding region
Neuro-Ophthalmic Disorders NGS Panel Fulgent Genetics United States	52	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States	563	241	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Combined Pituitary Hormone Deficiency NGS Panel Fulgent Genetics United States	10	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel Fulgent Genetics United States	244	78	D Deletion/duplication analysis C Sequence analysis of the entire coding region
COMBINED PITUITARY HORMONE DEFICIENCY Laboratorio de Genetica Clinica SL Spain	6	6	C Sequence analysis of the entire coding region
Combined Pituitary Hormone Deficiency Asper Biogene Asper Biogene LLC Estonia	10	8	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Septo-optic dysplasia Molecular Vision Laboratory United States	12	4	C Sequence analysis of the entire coding region
Single gene testing OTX2 CeGaT GmbH Germany	2	1	C Sequence analysis of the entire coding region
Developmental Eye Disease panel Molecular Vision Laboratory United States	107	59	C Sequence analysis of the entire coding region
OTX2 MGZ Medical Genetics Center Germany	3	1	C Sequence analysis of the entire coding region
Male Factor Infertility Asper Biogene Asper Biogene LLC Estonia	99	90	C Sequence analysis of the entire coding region T Targeted variant analysis
OTX2 Single Gene Fulgent Genetics United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5128	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Septo-optic Dysplasia NGS Panel Fulgent Genetics United States	15	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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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.