Clinical and research tests for 21 - Genetic Testing Registry (GTR) - NCBI

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Results: 41 to 60 of 63

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States	1	1722	C Sequence analysis of the entire coding region
Sufactant metabolism dysfunction, pulmonary: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	5	5	C Sequence analysis of the entire coding region
Pulmonary Surfactant Metabolism Dysfunction and Related Disorders, Panel Massive Sequencing (NGS) 6 Genes Reference Laboratory Genetics Spain	6	6	C Sequence analysis of the entire coding region
Familial Pulmonary Fibrosis and Pulmonary Surfactant Metabolism Dysfunction , Panel Massive Sequencing (NGS) 9 Genes Reference Laboratory Genetics Spain	8	9	C Sequence analysis of the entire coding region
INTERSTITIAL PULMONARY DISEASE ( PULMONARY SURFACTANT DYSFUNCTION) Laboratorio de Genetica Clinica SL Spain	3	3	C Sequence analysis of the entire coding region
Surfactant Dysfunction & Respiratory Distress in Premature Infants NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	12	11	C Sequence analysis of the entire coding region
Hermansky-Pudlak Syndrome & Pulmonary Fibrosis NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	36	40	C Sequence analysis of the entire coding region
Pulmonary Arterial Hypertension NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	20	22	C Sequence analysis of the entire coding region
Comprehensive Pulmonary NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	123	124	C Sequence analysis of the entire coding region
Pulmonary Surfactant Metabolism Dysfunction Type 3 , Sequencing ABCA3 Gene Reference Laboratory Genetics Spain	1	1	C Sequence analysis of the entire coding region
Comprehensive Pulmonary-Vascular Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	100	86	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neonatal Respiratory Distress Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	32	26	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neonatal Respiratory Distress - Surfactant Dysfunction Panel Blueprint Genetics Finland	3	5	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Interstitial Lung Disease Panel Blueprint Genetics Finland	1	25	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Pulmonology Panel Blueprint Genetics Finland	5	66	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hermansky-Pudlak Syndrome Panel Blueprint Genetics Finland	1	23	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Hematology Panel Blueprint Genetics Finland	4	239	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Surfactant metabolism dysfunction, pulmonary, type 3 Bioarray Spain	1	1	D Deletion/duplication analysis
Single gene testing ABCA3 CeGaT GmbH Germany	1	1	C Sequence analysis of the entire coding region
ABCA3 Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 41 to 60 of 63

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.