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The Turkish Journal of Pediatrics|September 9, 2008
Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritanceG Eda Utine, Yasemin Alanay, Dilek Aktaş, et al.Clinical Dysmorphology|March 14, 2007
Cerebro-facio-thoracic dysplasia: expanding the phenotypeDeirdre Cilliers, Yasemin Alanay, Koray Boduroglu, et al.Journal of Neurosurgery|December 25, 2007
Dynamic cervicomedullary cord compression and alterations in cerebrospinal fluid dynamics in children with achondroplasia. Report of four casesMoise Danielpour, William R Wilcox, Yasemin Alanay, et al.The Journal of Craniofacial Surgery|September 7, 2010
Intracranial and extracranial malformations in patients with craniofacial anomaliesGökhan Tunçbilek, Yasemin Alanay, Hakan Uzun, et al.The Turkish Journal of Pediatrics|June 28, 2012
Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 geneEsra Kiliç, Yasemin Alanay, Eda Utine, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 15, 2023
DNAJC21-related thrombocytopenia in a young adult femaleDeniz Aslan, Ozlem Akgun-Dogan, Beril Ay, et al.Annals of the New York Academy of Sciences|December 7, 2007
The skeletal dysplasias: clinical-molecular correlationsDavid L Rimoin, Daniel Cohn, Deborah Krakow, et al.The Turkish Journal of Pediatrics|October 13, 2009
Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromesPelin Ozlem Simşek, Gülen Eda Utine, Ayfer Alikaşifoğlu, et al.American Journal of Medical Genetics. Part A|June 11, 2005
Is Dandy-Walker malformation associated with "distal 13q deletion syndrome"? Findings in a fetus supporting previous observationsYasemin Alanay, Dilek Aktaş, Eda Utine, et al.European Journal of Medical Genetics|September 25, 2024
ITGB4-Related pyloric atresia without epidermolysis in two siblingsLamiya Aliyeva, Serdar Beken, Hanifenur Mancilar, et al.Pageof 15