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Filiz Hazan

Showing results (1-10 of 53) with videos related to

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Psychiatric Genetics|September 20, 2022
Novel RPS6KA3 mutations cause Coffin-Lowry syndrome in two patients and concurrent compulsive eyebrow-pulling behavior in one of themSemra Gürsoy, Filiz Hazan, Elif Çetinoğlu
Maedica|September 8, 2017
A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42Ali Vahabi, Filiz Hazan, Isa Abdi Rad
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 19, 2023
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndromeCeren Yılmaz Uzman, Semra Gürsoy, Filiz Hazan
Molecular Syndromology|February 6, 2020
Novel Ocular and Inner Ear Anomalies in a Patient with Myhre SyndromeSemra Gürsoy, Filiz Hazan, Tülay Öztürk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2013
Attempted suicide with levothyroxine in an adolescent girlHuseyin Anil Korkmaz, Ceyhun Dizdarer, Filiz Hazan, et al.
Journal of Clinical Research in Pediatric Endocrinology|November 15, 2012
Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3Hüseyin Anıl Korkmaz, Filiz Hazan, Ceyhun Dizdarer, et al.
Molecular Syndromology|October 4, 2021
Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel <i>EFNB1</i> Gene MutationSemra Gürsoy, Filiz Hazan, Tülay Öztürk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 19, 2024
A rare case of skeletal dysplasia: biallelic variant in <i>ACAN</i> geneGülçin Arslan, Filiz Hazan, Gülin Tabanlı, et al.
The Turkish Journal of Pediatrics|January 29, 2020
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndromeSemra Gürsoy, Yaşar Bekir Kutbay, Taha Reşid Özdemir, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 8, 2022
Screening of non-syndromic early-onset child and adolescent obese patients in terms of <i>LEP, LEPR, MC4R</i> and <i>POMC</i> gene variants by next-generation sequencingÖzlem Nalbantoğlu, Filiz Hazan, Sezer Acar, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Psychiatric Genetics|September 20, 2022
Novel RPS6KA3 mutations cause Coffin-Lowry syndrome in two patients and concurrent compulsive eyebrow-pulling behavior in one of themSemra Gürsoy, Filiz Hazan, Elif Çetinoğlu
Maedica|September 8, 2017
A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42Ali Vahabi, Filiz Hazan, Isa Abdi Rad
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 19, 2023
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndromeCeren Yılmaz Uzman, Semra Gürsoy, Filiz Hazan
Molecular Syndromology|February 6, 2020
Novel Ocular and Inner Ear Anomalies in a Patient with Myhre SyndromeSemra Gürsoy, Filiz Hazan, Tülay Öztürk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2013
Attempted suicide with levothyroxine in an adolescent girlHuseyin Anil Korkmaz, Ceyhun Dizdarer, Filiz Hazan, et al.
Journal of Clinical Research in Pediatric Endocrinology|November 15, 2012
Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3Hüseyin Anıl Korkmaz, Filiz Hazan, Ceyhun Dizdarer, et al.
Molecular Syndromology|October 4, 2021
Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel <i>EFNB1</i> Gene MutationSemra Gürsoy, Filiz Hazan, Tülay Öztürk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 19, 2024
A rare case of skeletal dysplasia: biallelic variant in <i>ACAN</i> geneGülçin Arslan, Filiz Hazan, Gülin Tabanlı, et al.
The Turkish Journal of Pediatrics|January 29, 2020
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndromeSemra Gürsoy, Yaşar Bekir Kutbay, Taha Reşid Özdemir, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 8, 2022
Screening of non-syndromic early-onset child and adolescent obese patients in terms of <i>LEP, LEPR, MC4R</i> and <i>POMC</i> gene variants by next-generation sequencingÖzlem Nalbantoğlu, Filiz Hazan, Sezer Acar, et al.
Pageof 6