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Filiz Hazan

Showing results (11-20 of 53) with videos related to

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The Journal of Clinical Pediatric Dentistry|November 9, 2020
Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric StudySemra Gürsoy, Filiz Hazan, Bülent Kaderli, et al.
Molecular Vision|February 5, 2013
A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1Filiz Hazan, A Taylan Ozturk, Hamit Adibelli, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 20, 2013
A case of Turner syndrome with concomitant transient hypogammaglobulinaemia of infancy and central diabetes insipidusHüseyin Anıl Korkmaz, Behzat Özkan, Filiz Hazan, et al.
Archivos Argentinos De Pediatria|November 22, 2016
Trichorhinophalangeal syndrome type II presenting with short stature in a childFiliz Hazan, Hüseyin A Korkmaz, Kanay Yararbaş, et al.
Central-European Journal of Immunology|May 20, 2020
Do microdeletions lead to immune deficiency?Sait Karaman, Filiz Hazan, Semiha Bahçeci Erdem, et al.
Molecular Syndromology|July 7, 2025
Pamidronate Treatment of a Patient with Opsismodysplasia and a Novel INPPL1 Variant: Efficacy, Mechanism, and Clinical OutcomesGulin Tabanli, Filiz Hazan, Gulsen Ozer, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 26, 2019
Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel <i>KISS1R/GPR54</i> Loss-of-Function MutationÖzlem Nalbantoğlu, Gülçin Arslan, Özge Köprülü, et al.
Journal of Neurology|March 12, 2009
Pontocerebellar hypoplasia type III (CLAM): extended phenotype and novel molecular findingsBurak Durmaz, Bernd Wollnik, Ozgur Cogulu, et al.
American Journal of Medical Genetics. Part A|June 2, 2012
A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous familyFiliz Hazan, Pia Ostergaard, Taylan Ozturk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 22, 2016
A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanelErhan Parıltay, Filiz Hazan, Esra Ataman, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
The Journal of Clinical Pediatric Dentistry|November 9, 2020
Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric StudySemra Gürsoy, Filiz Hazan, Bülent Kaderli, et al.
Molecular Vision|February 5, 2013
A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1Filiz Hazan, A Taylan Ozturk, Hamit Adibelli, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 20, 2013
A case of Turner syndrome with concomitant transient hypogammaglobulinaemia of infancy and central diabetes insipidusHüseyin Anıl Korkmaz, Behzat Özkan, Filiz Hazan, et al.
Archivos Argentinos De Pediatria|November 22, 2016
Trichorhinophalangeal syndrome type II presenting with short stature in a childFiliz Hazan, Hüseyin A Korkmaz, Kanay Yararbaş, et al.
Central-European Journal of Immunology|May 20, 2020
Do microdeletions lead to immune deficiency?Sait Karaman, Filiz Hazan, Semiha Bahçeci Erdem, et al.
Molecular Syndromology|July 7, 2025
Pamidronate Treatment of a Patient with Opsismodysplasia and a Novel INPPL1 Variant: Efficacy, Mechanism, and Clinical OutcomesGulin Tabanli, Filiz Hazan, Gulsen Ozer, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 26, 2019
Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel <i>KISS1R/GPR54</i> Loss-of-Function MutationÖzlem Nalbantoğlu, Gülçin Arslan, Özge Köprülü, et al.
Journal of Neurology|March 12, 2009
Pontocerebellar hypoplasia type III (CLAM): extended phenotype and novel molecular findingsBurak Durmaz, Bernd Wollnik, Ozgur Cogulu, et al.
American Journal of Medical Genetics. Part A|June 2, 2012
A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous familyFiliz Hazan, Pia Ostergaard, Taylan Ozturk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 22, 2016
A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanelErhan Parıltay, Filiz Hazan, Esra Ataman, et al.
Pageof 6