A novel AXIN2 gene mutation in sagittal synostosis von Yilmaz, Elanur, Mihci, Ercan, Guzel Nur, Banu, Alper, Ozgul M.

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Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene von Güzel Nur, Banu, Çelmeli, Gamze, Manguoğlu, Esra, Soyucen, Erdoğan, Bircan, İffet, Mıhçı, Ercan

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Interleukin-6 Gene Polymorphism in Febrile Seizures von Nur, Banu Guzel, MD, Kahramaner, Zelal, MD, Duman, Ozgur, MD, Dundar, Nihal Olgac, MD, Sallakc, Nilgun, MSc, Yavuzer, Ugur, MD, PhD, Haspolat, Senay, MD

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Bone mineral density in patients with mucopolysaccharidosis type III von Nur, Banu Guzel, Nur, Hakan, Mihci, Ercan

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A novel mutation in RNU4ATAC in a patient with microcephalic osteodysplastic primordial dwarfism type I von Kilic, Esra, Yigit, Gökhan, Utine, Gülen Eda, Wollnik, Bernd, Mihci, Ercan, Nur, Banu Güzel, Boduroglu, Koray

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Epidural capillary hemangioma: A review of the literature von Gencpinar, Pinar, Açıkbaş, Sabri Cem, Nur, Banu Güzel, Karaali, Kamil, Arslan, Murat, Gurer, Elif Inanc, Duman, Ozgur, Haspolat, Senay

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Celiac disease in patients with Williams-Beuren syndrome von Mıhçı, Ercan, Nur, Banu Güzel, Berker-Karaüzüm, Sibel, Yılmaz, Aygen, Artan, Reha

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Possible autosomal recessive inheritance in an infant with acrofacial dysostosis similar to nager syndrome von Nur, Banu Guzel, Bernier, Francois P., Oztekin, Osman, Kardelen, Fırat, Kalay, Salih, Parboosingh, Jillian S., Mihci, Ercan

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Associations between the clinical findings of cases having submicroscopic chromosomal imbalances at chromosomal breakpoints of apparently balanced structural rearrangements von Yakut, Sezin, Cetin, Zafer, Altiok Clark, Ozden, Guzel Nur, Banu, Mihci, Ercan, Berker Karauzum, Sibel

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Poland Syndrome in Childhood: Evaluation of the Clinical Findings von Güzel Nur, Banu, İbişoğlu, Zeynep, Mıhçı, Ercan

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Bilateral congenital cataracts in an infant with Klinefelter syndrome von Nur, Banu Güzel, Altıok-Clark, Özden, İlhan, Hatice Deniz, Sayar, Ersin, Yücel, İclal, Mıhçı, Ercan

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TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosis von Koçak, Gamze, Güzel, Banu Nur, Mıhçı, Ercan, Küpesiz, Osman Alphan, Yalçın, Koray, Manguoğlu, Ayşe Esra

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The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation von Nur, Banu Güzel, Altıok-Clark, Ozden, Toylu, Aslı, Lüleci, Güven, Mıhçı, Ercan

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Vertigo in Childhood: Evaluation of Clinical and Laboratory Findings von ERDOĞAN, Elvan, GÜZEL NUR, Banu, OLGAÇ DÜNDAR, Nihal

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Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation von Nur, Banu Guzel, Gencpinar, Pinar, Yuzbasıoglu, Ayse, Emre, Serap Dokmeci, Mihci, Ercan

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A familial interstitial 4q35 deletion with no discernible clinical effects von Yakut, Sezin, Clarck, Ozden Altiok, Sanhal, Cem, Nur, Banu Guzel, Mendilcioglu, Inanc, Karauzum, Sibel Berker, Cetin, Zafer

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Neonatal multiple sulfatase deficiency with a novel mutation and review of the literature von Nur, Banu Güzel, Mıhçı, Ercan, Pepe, Stefano, Biberoğlu, Gürsel, Ezgü, Fatih Süheyl, Ballabio, Andrea, Öztekin, Osman, Dursun, Oğuz

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Evaluation of the Response to the First Two Years of Growth Hormone Treatment in Kabuki Make-Up Syndrome von Celmeli, Gamze, Parlak, Mesut, Nur, Banu Guzel, Mihci, Ercan, Akcurin, Sema, Bircan, Iffet

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Evaluation of the Response to the First Two Years of Growth Hormone Treatment in Kabuki Make-Up Syndrome von Çelmeli, Gamze, Parlak, Mesut, Banu Güzel Nur, Mihçi, Ercan, Akçurin, Sema, İffet Bircan

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An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene von Nur, Banu Güzel, Çelmeli, Gamze, Soyuçen, Erdogan, Bircan, Iffet, Mihçi, Ercan

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