A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM \#612582)

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dc.contributor.authorErgin, R. N.
dc.contributor.authorCigerciogullari, E.
dc.contributor.authorAlanay, Y.
dc.contributor.authorYayla, M.
dc.date.accessioned2025-10-16T15:31:45Z
dc.date.issued2015
dc.identifier.otherWOS:000370466000012
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/9058
dc.publisherMEDECINE ET HYGIENE
dc.sourceGENETIC COUNSELING
dc.subjectFetus
dc.subjectMultiple abnormalities
dc.subject6p 24 deletion syndrome
dc.subjectPrenatal diagnosis
dc.subjectPrenatal Ultrasonography
dc.subjectGenetic testing
dc.titleA VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM \#612582)
dc.typeArticle

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