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	1.	Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey. [electronic resource] by Oğur, G Yüksel-Apak, M Demiryont, M Producer: 19901205 In: American journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Neu-Laxova syndrome: report of a case from Turkey. [electronic resource] by Kuseyri, F Bilge, I Bilgiç, L Apak, M Y Producer: 19931021 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of point mutations in Turkish DMD/BMD families using multiplex-single stranded conformation analysis (SSCA). [electronic resource] by Eraslan, S Kayserili, H Apak, M Y Kirdar, B Producer: 20000120 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Analysis of infertile brothers with congenital bilateral absence of vas deferens for mutations in the CFTR gene. [electronic resource] by Onay, T Kayserili, H Apak, M Y Kirdar, B Producer: 19990519 In: Clinical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Evaluation of the fetal kidney maturation by assessment of amniotic fluid alpha-1 microglobulin levels. [electronic resource] by Cağdaş, A Aydinli, K Irez, T Temizyürek, K Apak, M Y Producer: 20000627 In: European journal of obstetrics, gynecology, and reproductive biology vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR. [electronic resource] by Gökgöz, N Kuseyri, F Topaloğlu, H Yüksel-Apak, M Kirdar, B Producer: 19931021 In: Clinical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A familial Xp+ chromosome detected during fetal karyotyping, which is associated with short stature in four generations of a Turkish family. [electronic resource] by Karaman, B Wollnik, B Ermiş, H Yüksel-Apak, M Başaran, S Producer: 20031105 In: Prenatal diagnosis vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor. [electronic resource] by Utku, U Celik, Y Uyguner, O Yüksel-Apak, M Wollnik, B Producer: 20020306 In: European journal of neurology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Congenital insensitivity to pain with anyhydrosis: morphological studies of skin and peripheral nerves. [electronic resource] by Eker, R Apak, M Y Erbengi, T Apak, S Ozmen, M Producer: 19900214 In: The Turkish journal of pediatrics vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	10.	Glycine to tryptophan substitution in type I collagen in a patient with OI type III: a unique collagen mutation. [electronic resource] by Nuytinck, L Tükel, T Kayserili, H Apak, M Y De Paepe, A Producer: 20000717 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients. [electronic resource] by Savas, S Gokgoz, N Kayserili, H Ozkinay, F Yuksel-Apak, M Kirdar, B Producer: 20000525 In: Human heredity vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Tetra-amelia, lung hypo-/aplasia, cleft lip-palate, and heart defect: a new syndrome? [electronic resource] by Başaran, S Yüksel, A Ermiş, H Kuseyri, F Ağan, M Yüksel-Apak, M Producer: 19940808 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11. [electronic resource] by Dutly, F Baumer, A Kayserili, H Yüksel-Apak, M Zerova, T Hebisch, G Schinzel, A Producer: 19990602 In: American journal of medical genetics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Maternal uniparental disomy 22 has no impact on the phenotype. [electronic resource] by Schinzel, A A Basaran, S Bernasconi, F Karaman, B Yüksel-Apak, M Robinson, W P Producer: 19940204 In: American journal of human genetics vol. 54 Availability: No items available. Save to lists Add to cart (remove)
	15.	DNA analysis in Turkish Duchenne/Becker muscular dystrophy families. [electronic resource] by Battaloğlu, E Telatar, M Deymeer, F Serdaroğlu, P Kuseyri, F Ozdemir, C Apak, M Tolun, A Producer: 19920929 In: Human genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like features. [electronic resource] by Oğur, G Baykan, N De Paepe, A Steinmann, B Quatacker, J Kuseyrí, F Yüksel-Apak, M Producer: 19950418 In: Clinical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Prenatal diagnosis of hereditary spastic paraplegia. [electronic resource] by Hedera, P Williamson, J A Rainier, S Alvarado, D Tukel, T Apak, M Fink, J K Producer: 20010719 In: Prenatal diagnosis vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS). [electronic resource] by Kayserili, H Cox, T C Cox, L L Basaran, S Kiliç, G Ballabio, A Yüksel-Apak, M Producer: 20011011 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Carrier detection by DNA analysis in Duchenne muscular dystrophy families. [electronic resource] by Battaloğlu, E Telatar, M Deymeer, F Serdaroğlu, P Ozdemir, C Kuseyri, F Apak, M Y Tolun, A Producer: 19921217 In: The Turkish journal of pediatrics vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	20.	Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss. [electronic resource] by Uyguner, O Emiroglu, M Uzumcu, A Hafiz, G Ghanbari, A Baserer, N Yuksel-Apak, M Wollnik, B Producer: 20040218 In: Clinical genetics vol. 64 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 41 results.