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	1.	Celiac disease screening in 100 Turkish children with Down syndrome. [electronic resource] by Alanay, Yasemin Boduroğlu, Koray Tunçbilek, Ergül Producer: 20050901 In: The Turkish journal of pediatrics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	2.	A case of Sotos syndrome with 5q35 microdeletion and novel clinical findings. [electronic resource] by Kılıç, Esra Utine, Gülen Eda Boduroğlu, Koray Producer: 20131203 In: The Turkish journal of pediatrics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	3.	Oculo-palato-cerebral syndrome: a third case supporting autosomal recessive inheritance. [electronic resource] by Alanay, Yasemin Boduroglu, Koray Sönmez, Bariş Orhan, Mehmet Producer: 20041119 In: American journal of medical genetics. Part A vol. 130A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish women. [electronic resource] by Boduroğlu, Koray Alanay, Yasemin Koldan, Berrin Tunçbilek, Ergül Producer: 20041109 In: American journal of medical genetics. Part A vol. 127A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson Syndrome. [electronic resource] by Kilic, Esra Cetinkaya, Arda Utine, Gülen Eda Boduroğlu, Koray Producer: 20171220 In: Journal of child neurology vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma. [electronic resource] by Tarlan, Berçin Kiratli, Hayyam Kılıç, Esra Utine, Eda Boduroğlu, Koray Producer: 20150420 In: Ophthalmic genetics vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Cervical diastematomyelia in cervico-oculo-acoustic (Wildervanck) syndrome: MRI findings. [electronic resource] by Balci, Sevim Oguz, Kader Karli Firat, M Murat Boduroglu, Koray Producer: 20030303 In: Clinical dysmorphology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population. [electronic resource] by Boduroğlu, Koray Alanay, Yasemin Alikaşifoğlu, Mehmet Aktaş, Dilek Tunçbilek, Ergül Producer: 20060110 In: The Turkish journal of pediatrics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	9.	Barraquer-Simons syndrome: a rare clinical entity. [electronic resource] by Simsek-Kiper, Pelin Ozlem Roach, Emir Utine, Gulen Eda Boduroglu, Koray Producer: 20150818 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Partial distal aphalangia, duplication of metatarsal IV, microcephaly and borderline intelligence: a third patient suggesting autosomal recessive inheritance. [electronic resource] by Utine, Gülen Eda Alanay, Yasemin Aktaş, Dilek Alikaşifoğlu, Mehmet Boduroğlu, Koray Producer: 20090730 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritance. [electronic resource] by Kiper, Pelin Özlem Şimşek Utine, Gülen Eda Boduroğlu, Koray Alanay, Yasemin Producer: 20120209 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Prenatal diagnosis in a fetus with de-novo 20q11.2q13.1 deletion and review of the literature. [electronic resource] by Turgal, Mert Ozyuncu, Ozgur Utine, G Eda Kilic, Esra Boduroglu, Koray Producer: 20150113 In: Clinical dysmorphology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A novel de novo mutation involving the MLL2 gene in a Kabuki syndrome patient presenting with seizures. [electronic resource] by Bekircan-Kurt, Can Ebru Şimşek-Kiper, Pelin Özlem Boduroğlu, Koray Dericioğlu, Neşe Producer: 20170626 In: The Turkish journal of pediatrics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Anauxetic dysplasia: A rare clinical entity. [electronic resource] by Akgün-Doğan, Özlem Şimsek-Kiper, Pelin Özlem Utine, Gülen Eda Boduroğlu, Koray Producer: 20190116 In: The Turkish journal of pediatrics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Cerebro-facio-thoracic dysplasia: expanding the phenotype. [electronic resource] by Cilliers, Deirdre Alanay, Yasemin Boduroglu, Koray Utine, Eda Tunçbilek, Ergül Clayton-Smith, Jill Producer: 20070518 In: Clinical dysmorphology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A de novo 11q23 deletion in a patient presenting with severe ophthalmologic findings, psychomotor retardation and facial dysmorphism. [electronic resource] by Şimşek-Kiper, Pelin Özlem Bayram, Yavuz Ütine, Gülen Eda Alanay, Yasemin Boduroğlu, Koray Producer: 20150922 In: The Turkish journal of pediatrics vol. 56 Availability: No items available. Save to lists Add to cart (remove)
	17.	Intrafamilial variability of XYLT2-related spondyloocular syndrome. [electronic resource] by Guleray, Naz Simsek Kiper, Pelin Ozlem Utine, Gulen Eda Boduroglu, Koray Alikasifoglu, Mehmet Producer: 20200206 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes. [electronic resource] by Simşek, Pelin Ozlem Utine, Gülen Eda Alikaşifoğlu, Ayfer Alanay, Yasemin Boduroğlu, Koray Kandemir, Nurgün Producer: 20091029 In: The Turkish journal of pediatrics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	19.	Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 gene. [electronic resource] by Kiliç, Esra Alanay, Yasemin Utine, Eda Ozgen-Mocan, Burçe Robinson, Peter N Boduroğlu, Koray Producer: 20120814 In: The Turkish journal of pediatrics vol. 54 Availability: No items available. Save to lists Add to cart (remove)
	20.	A Diagnosis to Consider in an Adult Patient with Facial Features and Intellectual Disability: Williams Syndrome. [electronic resource] by Doğan, Özlem Akgün Şimşek Kiper, Pelin Özlem Utine, Gülen Eda Alikaşifoğlu, Mehmet Boduroğlu, Koray Publication details: Korean journal of family medicine Mar 2017 In: Korean journal of family medicine vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 68 results.