Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes

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dc.contributor.authorBramswig, Nuria C.
dc.contributor.authorLuedecke, Hermann\\-Josef
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorAlbrecht, Beate
dc.contributor.authorBarthelmie, Alexander
dc.contributor.authorBoduroglu, Koray
dc.contributor.authorBraunholz, Diana
dc.contributor.authorCaliebe, Almuth
dc.contributor.authorChrzanowska, Krystyna H.
dc.contributor.authorCzeschik, Johanna Christina
dc.contributor.authorEndele, Sabine
dc.contributor.authorGraf, Elisabeth
dc.contributor.authorGuillen\\-Navarro, Encarna
dc.contributor.authorKiper, Pelin Ozlem Simsek
dc.contributor.authorLopez\\-Gonzalez, Vanesa
dc.contributor.authorParenti, Ilaria
dc.contributor.authorPozojevic, Jelena
dc.contributor.authorUtine, Gulen Eda
dc.contributor.authorWieland, Thomas
dc.contributor.authorKaiser, Frank J.
dc.contributor.authorWollnik, Bernd
dc.contributor.authorStrom, Tim M.
dc.contributor.authorWieczorek, Dagmar
dc.date.accessioned2025-10-16T15:31:03Z
dc.date.issued2015
dc.identifier.doi10.1007/s00439-015-1535-8
dc.identifier.otherWOS:000354196200003
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/8978
dc.publisherSPRINGER
dc.sourceHUMAN GENETICS
dc.titleExome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes
dc.typeArticle

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