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7 results found.

1.
Ordering Recommendation:   Detects exon-level losses or gains of DNA on the X chromosome in individuals with unexplained intellectual disability, autism-spectrum disorders or other X-linked conditions. For whole-genome coverage, refer to Cytogenomic SNP Microarray (2003414).
2.
Ordering Recommendation:   Use to determine X-chromosome inactivation (XCI) pattern for female carriers of X-linked disorders and assess pathogenicity of genetic variant in an X-linked gene. Test does not detect clonality.
3.
Ordering Recommendation:   Preferred test for individuals with suspected X-linked intellectual disability (XLID) when genomic microarray testing has not identified causal variant(s).
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Ordering Recommendation:   Nonstandard test for determining cause of malabsorption. Test evaluates carbohydrate absorption of the proximal small intestine. Refer to 5g dose testing for patients who do not tolerate the 25g dose.
6.
Ordering Recommendation:   Nonstandard test for determining cause of malabsorption. Test evaluates carbohydrate absorption of the proximal small intestine. 5g dose is preferred in patients who do not tolerate the 25g dose.
7.
Ordering Recommendation:   Nonstandard test for determining cause of malabsorption. Test evaluates carbohydrate absorption of the proximal small intestine.