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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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Labs matching your search
62 labs with tests matching your search, 2 labs matching in other ways
Results:
423 genetic tests from 62 labs with tests matching your search, 2 labs matching in other ways
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods | |
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| 15 | 20 |
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423 tests from 62 labs
Page 1 of 22❯Noonan Syndrome by Genome Diagnostics Laboratory, Hospital For Sick Children
14 conditions, 15 genes
14 conditions, 15 genes
NOONAN SYNDROME by Clinical Genomics Unit, Hospital Universitari Germans Trias i Pujol
5 conditions, 16 genes
5 conditions, 16 genes
Noonan syndrome by Dubai Health Genomic Medicine Center, Dubai Health
18 conditions, 18 genes
18 conditions, 18 genes
Noonan Syndrome by MGZ Medical Genetics Center
4 conditions, 9 genes
4 conditions, 9 genes
Noonan syndrome core NGS panel by HNL Genomics Connective Tissue Gene Tests
10 conditions, 14 genes
10 conditions, 14 genes
Noonan syndrome core Comprehensive panel by HNL Genomics Connective Tissue Gene Tests
10 conditions, 14 genes
10 conditions, 14 genes
Noonan syndrome core Deletion / Duplication panel by HNL Genomics Connective Tissue Gene Tests
10 conditions, 14 genes
10 conditions, 14 genes
Noonan syndrome 4, 610733, Autosomal dominant; NS4 (Noonan syndrome) (SOS1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 4, 610733, Autosomal dominant; NS4 (Noonan syndrome) (SOS1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan Syndrome and Related Panel by Mayo Clinic Laboratories, Mayo Clinic
15 conditions, 20 genes
15 conditions, 20 genes
Noonan syndrome 10, 616564, Autosomal dominant; NS10 (Noonan syndrome) (LZTR1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 3, 609942; NS3 (Noonan syndrome) (KRAS gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 8, 615355, Autosomal dominant; NS8 (Noonan syndrome) (RIT1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 3, 609942; NS3 (Noonan syndrome) (KRAS gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 9, 616559, Autosomal dominant; NS9 (Noonan syndrome) (SOS2 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 9, 616559, Autosomal dominant; NS9 (Noonan syndrome) (SOS2 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 7, 613706, Autosomal dominant; NS7 (Noonan syndrome) (BRAF gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 1, 163950, Autosomal dominant; NS1 (Noonan syndrome) (PTPN11 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 1, 163950, Autosomal dominant; NS1 (Noonan syndrome) (PTPN11 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
Noonan syndrome 8, 615355, Autosomal dominant; NS8 (Noonan syndrome) (RIT1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
1 condition, 1 gene
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.