When Genetic Testing Can't Find THE Answer: How Unique Clinical Presentations Challenge the Clinician
PúblicoMLA citation style (9th ed.)
. 2020. marian.palni-palci-staging.notch8.cloud/concern/generic_works/0537176f-10e4-4010-aada-2619a54cb276?locale=es. When Genetic Testing Can't Find The Answer: How Unique Clinical Presentations Challenge the Clinician.APA citation style (7th ed.)
(2020). When Genetic Testing Can't Find THE Answer: How Unique Clinical Presentations Challenge the Clinician. https://marian.palni-palci-staging.notch8.cloud/concern/generic_works/0537176f-10e4-4010-aada-2619a54cb276?locale=esChicago citation style (CMOS 17, author-date)
When Genetic Testing Can't Find The Answer: How Unique Clinical Presentations Challenge the Clinician. 2020. https://marian.palni-palci-staging.notch8.cloud/concern/generic_works/0537176f-10e4-4010-aada-2619a54cb276?locale=es.Note: These citations are programmatically generated and may be incomplete.
Multi-system disorders may be difficult to differentiate between, especially as genetic causes are still being defined and in light of phenotypic variability. We present a case of a teen with multiple congenital defects for which genetic testing was inconclusive, showing features of : Noonan Syndrome (NS), Mullerian duct aplasia-renal aplasia-cervicothoracic somite dysplasia (MURCS), and VACTERL association.
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Katelyn_Anne_Dato-on.pdf | 2021-10-22 | Público | Descargar |