Further expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome

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dc.contributor.authorSimsek\\-Kiper, Pelin Ozlem
dc.contributor.authorTaskiran, Ekim
dc.contributor.authorKosukcu, Can
dc.contributor.authorArslan, Umut Ece
dc.contributor.authorCormier\\-Daire, Valerie
dc.contributor.authorGonc, Nazli
dc.contributor.authorOzon, Alev
dc.contributor.authorAlikasifoglu, Ayfer
dc.contributor.authorKandemir, Nurgun
dc.contributor.authorUtine, Gulen Eda
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorAlikasifoglu, Mehmet
dc.contributor.authorBoduroglu, Koray
dc.date.accessioned2025-10-16T15:23:29Z
dc.date.issued2019
dc.identifier.doi10.1002/ajmg.a.61154
dc.identifier.otherWOS:000471068000008
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7994
dc.publisherWILEY
dc.sourceAMERICAN JOURNAL OF MEDICAL GENETICS PART A
dc.subject20p13p12.3 deletion
dc.subject3M syndrome
dc.subjectBMP2
dc.subjectCUL7
dc.subjectgenotype\\-phenotype correlation
dc.subjectOBSL1
dc.titleFurther expanding the mutational spectrum and investigation of genotype-phenotype correlation in 3M syndrome
dc.typeArticle

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