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Orphanet Journal of Rare Diseases|June 3, 2006
Congenital contractural arachnodactyly (Beals syndrome)Ergül Tunçbilek, Yasemin AlanayJournal of Clinical Research in Pediatric Endocrinology|December 29, 2025
Osteogenesis Imperfecta with Pes Equinovarus: A Rare Combination and a Rare Col1a1 VariantNurhan Özcan Murat, Yasemin AlanayJournal of Clinical Research in Pediatric Endocrinology|December 14, 2011
A review of the principles of radiological assessment of skeletal dysplasiasYasemin Alanay, Ralph S LachmanThe Turkish Journal of Pediatrics|August 2, 2005
Celiac disease screening in 100 Turkish children with Down syndromeYasemin Alanay, Koray Boduroğlu, Ergül TunçbilekClinical Dysmorphology|June 15, 2004
Noonan syndrome and systemic lupus erythematosus: presentation in childhoodYasemin Alanay, Sevim Balcı, Seza OzenThe Journal of Craniofacial Surgery|July 28, 2009
Le Fort III bipartition osteotomy to treat a rare craniofacial anomaly: frontofacionasal dysostosisGökhan Tunçbilek, Yasemin Alanay, Aycan KayikçioğluAmerican Journal of Medical Genetics. Part A|September 16, 2004
Oculo-palato-cerebral syndrome: a third case supporting autosomal recessive inheritanceYasemin Alanay, Koray Boduroglu, Bariş Sönmez, et al.BMC Medical Genomics|August 1, 2021
Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case reportTugce Bozkurt, Yasemin Alanay, Ugur Isik, et al.American Journal of Medical Genetics. Part A|April 23, 2004
Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish womenKoray Boduroğlu, Yasemin Alanay, Berrin Koldan, et al.Pediatric Dermatology|October 9, 2015
Hoyeraal-Hreidarsson Syndrome: An Extremely Rare Dyskeratosis Congenita PhenotypeÖzgür Bakar, Ugˇur Işik, Cengiz Canpolat, et al.Pageof 15