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Hatice Mutlu-Albayrak

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International Journal of Pediatric Otorhinolaryngology|December 23, 2018
Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 geneHatice Mutlu-Albayrak, Kadri Karaer
The Turkish Journal of Pediatrics|March 6, 2020
Schwartz Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutationGürkan Gürbüz, Hatice Mutlu Albayrak
Acta Neurologica Belgica|June 21, 2020
PIGA-related epileptic encephalopathy demonstrating intrafamilial phenotypic heterogeneityPeren Perk Yucel, Hatice Mutlu Albayrak
Molecular Syndromology|February 28, 2022
Kosaki Overgrowth Syndrome: Report of a Family with a Novel <i>PDGFRB</i> VariantHatice Mutlu Albayrak, Alistair D Calder
Pediatric Allergy, Immunology, and Pulmonology|August 3, 2022
Overview of the Pulmonary Manifestations in Patients with Autosomal Recessive Cutis Laxa Type ICHatice Mutlu-Albayrak, Nagehan Emiralioğlu, Çağrı Damar
Pediatrics and Neonatology|July 17, 2016
Fetal Valproate SyndromeHatice Mutlu-Albayrak, Cahide Bulut, Hüseyin Çaksen
Journal of Pediatric Genetics|August 14, 2019
Esophageal Atresia and Thenar Hypoplasia Associated with Asymmetric Crying FaceHatice Mutlu-Albayrak, Çağrı Damar, Gürkan Gürbüz
Neurogenetics|November 20, 2019
Childhood-onset autosomal recessive ataxias: a cross-sectional study from TurkeyHatice Mutlu-Albayrak, Emre Kırat, Gürkan Gürbüz
American Journal of Medical Genetics. Part A|May 5, 2021
From cataract to syndrome diagnosis: Revaluation of Warburg-Micro syndrome Type 1 patientsHatice Mutlu Albayrak, Nursel H Elçioğlu, Burcu Yeter, et al.
Turk Pediatri Arsivi|October 25, 2017
A congenital cranial dysinnervation disorder: Möbius' syndromeHatice Mutlu Albayrak, Nuriye Tarakçı, Hüseyin Altunhan, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
International Journal of Pediatric Otorhinolaryngology|December 23, 2018
Vocal cord immobility as a cause of aphonia in a child with 3p13p12 deletion syndrome encompassing FOXP1 geneHatice Mutlu-Albayrak, Kadri Karaer
The Turkish Journal of Pediatrics|March 6, 2020
Schwartz Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutationGürkan Gürbüz, Hatice Mutlu Albayrak
Acta Neurologica Belgica|June 21, 2020
PIGA-related epileptic encephalopathy demonstrating intrafamilial phenotypic heterogeneityPeren Perk Yucel, Hatice Mutlu Albayrak
Molecular Syndromology|February 28, 2022
Kosaki Overgrowth Syndrome: Report of a Family with a Novel <i>PDGFRB</i> VariantHatice Mutlu Albayrak, Alistair D Calder
Pediatric Allergy, Immunology, and Pulmonology|August 3, 2022
Overview of the Pulmonary Manifestations in Patients with Autosomal Recessive Cutis Laxa Type ICHatice Mutlu-Albayrak, Nagehan Emiralioğlu, Çağrı Damar
Pediatrics and Neonatology|July 17, 2016
Fetal Valproate SyndromeHatice Mutlu-Albayrak, Cahide Bulut, Hüseyin Çaksen
Journal of Pediatric Genetics|August 14, 2019
Esophageal Atresia and Thenar Hypoplasia Associated with Asymmetric Crying FaceHatice Mutlu-Albayrak, Çağrı Damar, Gürkan Gürbüz
Neurogenetics|November 20, 2019
Childhood-onset autosomal recessive ataxias: a cross-sectional study from TurkeyHatice Mutlu-Albayrak, Emre Kırat, Gürkan Gürbüz
American Journal of Medical Genetics. Part A|May 5, 2021
From cataract to syndrome diagnosis: Revaluation of Warburg-Micro syndrome Type 1 patientsHatice Mutlu Albayrak, Nursel H Elçioğlu, Burcu Yeter, et al.
Turk Pediatri Arsivi|October 25, 2017
A congenital cranial dysinnervation disorder: Möbius' syndromeHatice Mutlu Albayrak, Nuriye Tarakçı, Hüseyin Altunhan, et al.
Pageof 2