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Hülya Kayserili

Showing results (1-10 of 130) with videos related to

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The Turkish Journal of Pediatrics|October 13, 2009
Kabuki make-up syndrome with unilateral renal agenesisRasim Ozgür Rosti, Hülya Kayserili
Molecular Syndromology|June 16, 2022
A New Family with a Novel <i>OTUD6B</i> Mutation: Practicing Whole Exome Sequencing for Antenatal Diagnosis of Tetralogy of FallotEsra Börklü, Umut Altunoğlu, Serpil Eraslan, et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir|November 6, 2008
[A case of Hennekam syndrome presenting with massive pericardial effusion]Kemal Nişli, Naci Oner, Hülya Kayserili, et al.
American Journal of Medical Genetics. Part A|April 26, 2014
Mild nasal clefting may be predictive for ALX4 heterozygotesUmut Altunoglu, Bilge Satkın, Zehra Oya Uyguner, et al.
American Journal of Medical Genetics. Part A|April 15, 2016
Microcephaly, dysmorphic features, corneal dystrophy, hairy nipples, underdeveloped labioscrotal folds, and small cerebellum in four patientsHülya Kayserili, Umut Altunoglu, Gozde Yesil, et al.
Pediatric Neurology|June 13, 2006
Quadrigeminal cistern arachnoid cyst in a patient with Kabuki syndromeBülent Kara, Hülya Kayserili, Murat Imer, et al.
Journal of Medical Systems|December 1, 2011
Down syndrome diagnosis based on Gabor Wavelet TransformSafak Saraydemir, Necmi Taşpınar, Osman Eroğul, et al.
Pediatric Radiology|April 4, 2015
Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index fingerHiroko Yagi, Masaki Takagi, Yukihiro Hasegawa, et al.
Journal of the Turkish German Gynecological Association|March 5, 2014
Prenatal diagnosis of frontonasal dysplasia with anterior encephaloceleAytul Çorbacıoğlu Esmer, Ibrahim Kalelioğlu, Hülya Kayserili, et al.
American Journal of Medical Genetics. Part A|December 6, 2011
Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutationsHülya Kayserili, U Altunoglu, H Ozgur, et al.
Pageof 13

Showing results (1-10 of 130) with videos related to

Sort By:
Pageof 13
The Turkish Journal of Pediatrics|October 13, 2009
Kabuki make-up syndrome with unilateral renal agenesisRasim Ozgür Rosti, Hülya Kayserili
Molecular Syndromology|June 16, 2022
A New Family with a Novel <i>OTUD6B</i> Mutation: Practicing Whole Exome Sequencing for Antenatal Diagnosis of Tetralogy of FallotEsra Börklü, Umut Altunoğlu, Serpil Eraslan, et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir|November 6, 2008
[A case of Hennekam syndrome presenting with massive pericardial effusion]Kemal Nişli, Naci Oner, Hülya Kayserili, et al.
American Journal of Medical Genetics. Part A|April 26, 2014
Mild nasal clefting may be predictive for ALX4 heterozygotesUmut Altunoglu, Bilge Satkın, Zehra Oya Uyguner, et al.
American Journal of Medical Genetics. Part A|April 15, 2016
Microcephaly, dysmorphic features, corneal dystrophy, hairy nipples, underdeveloped labioscrotal folds, and small cerebellum in four patientsHülya Kayserili, Umut Altunoglu, Gozde Yesil, et al.
Pediatric Neurology|June 13, 2006
Quadrigeminal cistern arachnoid cyst in a patient with Kabuki syndromeBülent Kara, Hülya Kayserili, Murat Imer, et al.
Journal of Medical Systems|December 1, 2011
Down syndrome diagnosis based on Gabor Wavelet TransformSafak Saraydemir, Necmi Taşpınar, Osman Eroğul, et al.
Pediatric Radiology|April 4, 2015
Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index fingerHiroko Yagi, Masaki Takagi, Yukihiro Hasegawa, et al.
Journal of the Turkish German Gynecological Association|March 5, 2014
Prenatal diagnosis of frontonasal dysplasia with anterior encephaloceleAytul Çorbacıoğlu Esmer, Ibrahim Kalelioğlu, Hülya Kayserili, et al.
American Journal of Medical Genetics. Part A|December 6, 2011
Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutationsHülya Kayserili, U Altunoglu, H Ozgur, et al.
Pageof 13