Works by Hazan, Filiz

Results: 55

Phenotypic spectrum of CHARGE syndrome based on clinical characteristics.

Published in:

Turkish Journal of Medical Sciences, 2018, v. 48, n. 5, p. 911, doi. 10.3906/sag-1611-107

By:

AKSEL KILIÇARSLAN, Özge;
ATAMAN, Esra;
GÜRSOY, Semra;
HAZAN, Filiz;
RANDA, Cemre;
ÇANKAYA, Tufan;
ERÇAL, Derya;
ÜLGENALP, Ayfer;
GİRAY BOZKAYA, Özlem

Publication type:

Article

Do microdeletions lead to immune deficiency?

Published in:

Central European Journal of Immunology, 2020, v. 45, n. 1, p. 69, doi. 10.5114/ceji.2020.94671

By:

KARAMAN, SAIT;
HAZAN, FILIZ;
ERDEM, SEMIHA BAHÇECI;
GÜLEZ, NESRIN;
GENEL, FERAH

Publication type:

Article

Clinical features and molecular genetics of patients with RASopathies: expanding the phenotype with rare genes and novel variants.

Published in:

European Journal of Pediatrics, 2025, v. 184, n. 1, p. 1, doi. 10.1007/s00431-024-05825-8

By:

Yılmaz Uzman, Ceren;
Gürsoy, Semra;
Özkan, Behzat;
Vuran, Gamze;
Ayyıldız Emecen, Durdugül;
Köprülü, Özge;
Bilen, Mertkan Mustafa;
Hazan, Filiz

Publication type:

Article

A rare case of skeletal dysplasia: biallelic variant in ACAN gene.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2024, v. 37, n. 12, p. 1104, doi. 10.1515/jpem-2024-0255

By:

Arslan, Gülçin;
Hazan, Filiz;
Tabanlı, Gülin;
Kırkgöz, Tarık;
Özkan, Behzat

Publication type:

Article

Identification of a novel homozygous NR5A1 variant in a patient with a 46,XY disorders of sex development.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2024, v. 37, n. 6, p. 575, doi. 10.1515/jpem-2023-0551

By:

Kırkgöz, Tarık;
Gürsoy, Semra;
Acar, Sezer;
Köprülü, Özge;
Özkaya, Beyhan;
Arslan, Gülçin;
Nalbantoğlu, Özlem;
Hazan, Filiz;
Özkan, Behzat

Publication type:

Article

Screening of non-syndromic early-onset child and adolescent obese patients in terms of LEP, LEPR, MC4R and POMC gene variants by next-generation sequencing.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 8, p. 1041, doi. 10.1515/jpem-2022-0027

By:

Nalbantoğlu, Özlem;
Hazan, Filiz;
Acar, Sezer;
Gürsoy, Semra;
Özkan, Behzat

Publication type:

Article

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1111, doi. 10.1515/jpem-2015-0482

By:

Parıltay, Erhan;
Hazan, Filiz;
Ataman, Esra;
Demir, Korcan;
Etlik, Özdal;
Özbek, Erhan;
Özkan, Behzat

Publication type:

Article

Two different patterns of mini-puberty in two 46,XY newborns with 17β-hydroxysteroid dehydrogenase type 3 deficiency.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 7/8, p. 961, doi. 10.1515/jpem-2014-0365

By:

Demir, Korcan;
Yıldız, Melek;
Elmas, Özlem Nalbantoğlu;
Korkmaz, Hüseyin Anıl;
Tunç, Selma;
Olukman, Özgür;
Hazan, Filiz;
Özkan, Keramettin Uğur;
Özkan, Behzat

Publication type:

Article

Attempted suicide with levothyroxine in an adolescent girl.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 129, doi. 10.1515/jpem-2012-0247

By:

Korkmaz, Huseyin Anil;
Dizdarer, Ceyhun;
Hazan, Filiz;
Karaarslan, Utku

Publication type:

Article

The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome.

Published in:

Turkish Journal of Pediatrics, 2019, v. 61, n. 4, p. 589, doi. 10.24953/turkjped.2019.04.017

By:

Gürsoy, Semra;
Kutbay, Yaşar Bekir;
Özdemir, Taha Reşid;
Hazan, Filiz

Publication type:

Article

Kromozom 22q11.2 Delesyon Sendromu Tanılı Hastaların Klinik ve Laboratuvar Özellikleri.

Published in:

Turkiye Klinikleri Journal of Pediatrics / Türkiye Klinikleri Pediatri Dergisi, 2021, v. 30, n. 2, p. 117, doi. 10.5336/pediatr.2021-81283

By:

HAZAN, Filiz;
NALBANTOĞLU, Özlem;
GÜRSOY, Semra;
ÖZEN, Selime;
YILMAZER, Murat Muhtar;
GENEL, Ferah;
MEŞE, Timur;
ÖZKAN, Behzat

Publication type:

Article

Acrocallosal Syndrome First Presenting with Acute Lymphoblastic Leukemia: A Rare Case Report.

Published in:

2019

By:

Koker, Sultan;
Hazan, Filiz;
Oymak, Yeşim;
Soydan, Ekin;
Karapınar, Tuba;
Ay, Yılmaz;
Demirağ, Bengü;
Vergin, Raziye;
Koker, Sultan Aydin;
Karapınar, Tuba Hilkay;
Vergin, Raziye Canan

Publication type:

Case Study

SCOT DEFICIENCY MIMICKING SEPSIS: AN UNUSUAL CAUSE OF INCREASED ANION GAP METABOLIC ACIDOSIS.

Published in:

Journal of Basic & Clinical Health Sciences, 2024, v. 8, n. 2, p. 507, doi. 10.30621/jbachs.1217436

By:

Kisa, Pelin Teke;
Gursoy, Semra;
Seven, Pınar;
Pirinc, Neslihan;
Sandal, Ozlem Sarac;
Atakul, Gulhan;
Hazan, Filiz;
Tanyalcin, Tijen

Publication type:

Article

Histopathological and Genetic Features of Patients with Limb Girdle Muscular Dystrophy Type 2C.

Published in:

Turkish Journal of Pathology, 2014, v. 30, n. 2, p. 111, doi. 10.5146/tjpath.2014.01239

By:

DİNİZ, Gülden;
HAZAN, Filiz;
TOSUN YILDIRIM, Hülya;
ÜNALP, Aycan;
POLAT, Muzaffer;
SERDA ROĞLU, Gül;
GÜZEL, Orkide;
BAĞ, Özlem;
SEÇİL, Yaprak;
ÖZGÖNÜL, Figen;
TÜRE, Sabiha;
AKHAN, Galip;
TÜKÜN, Ajlan

Publication type:

Article

A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42.

Published in:

Maedica - a Journal of Clinical Medicine, 2017, v. 12, n. 1, p. 62

By:

VAHABI, Ali;
HAZAN, Filiz;
RAD, Isa Abdi

Publication type:

Article

Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 4, p. 358, doi. 10.4274/jcrpe.galenos.2020.2019.0001

By:

Gürsoy, Semra;
Hazan, Filiz;
Aykut, Ayça;
Nalbantoğlu, Özlem;
Korkmaz, Hüseyin Anıl;
Demir, Korcan;
Özkan, Behzat;
Çoğulu, Özgür

Publication type:

Article

Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of- Function Mutation.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 4, p. 444, doi. 10.4274/jcrpe.galenos.2019.2018.0230

By:

Nalbantoğlu, Özlem;
Arslan, Gülçin;
Köprülü, Özge;
Hazan, Filiz;
Gürsoy, Semra;
Özkan, Behzat

Publication type:

Article

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 3, p. 216, doi. 10.4274/jcrpe.4225

By:

Tunç, Selma;
Demir, Korcan;
Tükün, Fatma Ajlan;
Topal, Cihan;
Hazan, Filiz;
Sağlam, Burcu;
Nalbantoğlu, Özlem;
Yıldız, Melek;
Özkan, Behzat

Publication type:

Article

A Case with Infantile-Onset Pancytopenia and Hyperglycemia Associated with SLC19A2 Mutation.

Published in:

2015

By:

Katipoğlu, Nagehan;
Karapınar, Tuba Hilkay;
Demir, Korcan;
Köker, Sultan Aydın;
Nalbantoğlu, Özlem;
Ay, Yılmaz;
Korkmaz, Hüseyin Anıl;
Oymak, Yeşim;
Yıldız, Melek;
Özcan, Esin;
Tunç, Selma;
Hazan, Filiz;
Vergin, Canan;
Özkan, Behzat

Publication type:

Abstract

Phenotype-Genotype Correlations in Bardet-Biedl Syndrome Patients with Molecular Analysis.

Published in:

2015

By:

Solmaz, Aslı Ece;
Onay, Hüseyin;
Atık, Tahir;
Aykut, Ayça;
Güneş, Meltem Cerrah;
Yüreğir, Özge Özalp;
Baş, Veysel Nijat;
Hazan, Filiz;
Kırbıyık, Özgür;
Özkınay, Ferda

Publication type:

Abstract

A Case with Acrodysostosis and Hormone Resistance.

Published in:

2015

By:

Tunç, Selma;
Demir, Korcan;
Hazan, Filiz;
Kırbıyık, Özgür;
Soyaltın, Eren;
Elmas, Özlem Nalbantoğlu;
Yıldız, Melek;
Korkmaz, Hüseyin Anıl;
Özkan, Behzat

Publication type:

Abstract

Screening of PROP-1, LHX2, and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland.

Published in:

2015

By:

Korkmaz, Hüseyin Anıl;
Karaarslan, Utku;
Eraslan, Cenk;
Atila, Dinçer;
Hazan, Filiz;
Barışık, Vatan;
Ata, Emine Sevcan;
Etlik, Özdal;
Yıldız, Melek;
Özkan, Behzat

Publication type:

Abstract

46,XY Complete Gonadal Dysgenesis: A Case Report.

Published in:

2015

By:

Korkmaz, Hüseyin Anıl;
Yıldız, Melek;
Hazan, Filiz;
Demir, Korcan;
Tunç, Selma;
Elmas, Özlem Nalbantoğlu;
Özkan, Behzat

Publication type:

Abstract

A Case with Infantile-Onset Pancytopenia and Hyperglycemia Associated with SLC19A2 Mutation.

Published in:

2015

By:

Katipoğlu, Nagehan;
Karapınar, Tuba Hilkay;
Demir, Korcan;
Köker, Sultan Aydın;
Nalbantoğlu, Özlem;
Ay, Yılmaz;
Korkmaz, Hüseyin Anıl;
Oymak, Yeşim;
Yıldız, Melek;
Özcan, Esin;
Tunç, Selma;
Hazan, Filiz;
Vergin, Canan;
Özkan, Behzat

Publication type:

Case Study

Phenotype-Genotype Correlations in Bardet-Biedl Syndrome Patients with Molecular Analysis.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 82

By:

Solmaz, Aslı Ece;
Onay, Hüseyin;
Atık, Tahir;
Aykut, Ayça;
Güneş, Meltem Cerrah;
Yüreğir, Özge Özalp;
Baş, Veysel Nijat;
Hazan, Filiz;
Kırbıyık, Özgür;
Özkınay, Ferda

Publication type:

Article

A Case with Acrodysostosis and Hormone Resistance.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 75

By:

Tunç, Selma;
Demir, Korcan;
Hazan, Filiz;
Kırbıyık, Özgür;
Soyaltın, Eren;
Elmas, Özlem Nalbantoğlu;
Yıldız, Melek;
Korkmaz, Hüseyin Anıl;
Özkan, Behzat

Publication type:

Article

46,XY Complete Gonadal Dysgenesis: A Case Report.

Published in:

2015

By:

Korkmaz, Hüseyin Anıl;
Yıldız, Melek;
Hazan, Filiz;
Demir, Korcan;
Tunç, Selma;
Elmas, Özlem Nalbantoğlu;
Özkan, Behzat

Publication type:

Case Study

Screening of PROP-1, LHX2, and POU1F1 Mutations in Patients with Ectopic Posterior Pituitary Gland.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 65

By:

Korkmaz, Hüseyin Anıl;
Karaarslan, Utku;
Eraslan, Cenk;
Atila, Dinçer;
Hazan, Filiz;
Barışık, Vatan;
Ata, Emine Sevcan;
Etlik, Özdal;
Yıldız, Melek;
Özkan, Behzat

Publication type:

Article

A Case of Turner Syndrome with Concomitant Transient Hypogammaglobulinaemia of Infancy and Central Diabetes Insipidus.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2013, v. 5, n. 1, p. 62, doi. 10.4274/Jcrpe.880

By:

Korkmaz, Hüseyin Anıl;
Özkan, Behzat;
Hazan, Filiz;
Büyükinan, Muammer;
Çelik, Tanju

Publication type:

Article

Hypochondroplasia in a Child with 1620C>G (Asn540Lys) Mutation in FGFR3.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2012, v. 4, n. 4, p. 220, doi. 10.4274/Jcrpe.787

By:

Anıl Korkmaz, Hüseyin;
Hazan, Filiz;
Dizdarer, Ceyhun;
Tükün, Ajlan

Publication type:

Article

CYP4F22 Gene Mutations in Patients with Autosomal Recessive Congenital Ichthyosis: Identification of Two Novel Mutations.

Published in:

Turkish Journal of Dermatology / Turk Dermatoloji Dergisis, 2020, v. 14, n. 4, p. 90, doi. 10.4103/tjd.tjd_91_20

By:

Ateş, Esra Arslan;
Onay, Hüseyin;
Ertam, Ilgen;
Ataman, Esra;
Hazan, Filiz;
Durmaz, Asude;
Dereli, Tugrul;
Özkinay, Ferda

Publication type:

Article

Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.

Published in:

Acta Myologica, 2018, v. 37, n. 3, p. 210

By:

YİŞ, ULUÇ;
DİNİZ, GÜLDEN;
HAZAN, FILIZ;
MAGÜLER, HÜLYA SEVCAN DAI;
BAYSAL, BAHAR TOKLU;
BAYDAN, FIGEN;
AKINCI, GÜLÇIN;
ÜNALP, AYCAN;
AKTAN, GÜL.;
BAYRAM, ERHAN;
HIZ, SEMRA;
PAKETÇİ, CEM;
OKUR, DERYA;
ÖZER, ERDENER;
DANYELI, AYÇA ERSEN;
POLAT, MUZAFFER;
UYANIK, GöKHAN;
ÇIRAK, SEBAHATTIN

Publication type:

Article

Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric Study.

Published in:

2020

By:

Gürsoy, Semra;
Hazan, Filiz;
Kaderli, Bülent;
Meşe, Timur;
Tükün, Ajlan

Publication type:

journal article

Pontocerebellar hypoplasia type III (CLAM): Extended phenotype and novel molecular findings.

Published in:

Journal of Neurology, 2009, v. 256, n. 3, p. 416, doi. 10.1007/s00415-009-0094-0

By:

Durmaz, Burak;
Wollnik, Bernd;
Cogulu, Ozgur;
Yun Li;
Tekgul, Hasan;
Hazan, Filiz;
Ozkinay, Ferda

Publication type:

Article

Concomitant Alpha- and Gamma-Sarcoglycan Deficiencies in a Turkish Boy with a Novel Deletion in the Alpha-Sarcoglycan Gene.

Published in:

2014

By:

Diniz, Gulden;
Yildirim, Hulya Tosun;
Gokben, Sarenur;
Serdaroglu, Gul;
Hazan, Filiz;
Yararbas, Kanay;
Tukun, Ajlan

Publication type:

Case Study

Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations.

Published in:

2016

By:

Atik, Tahir;
Aykut, Ayca;
Hazan, Filiz;
Onay, Huseyin;
Goksen, Damla;
Darcan, Sukran;
Tukun, Ajlan;
Ozkinay, Ferda

Publication type:

journal article

A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall–Smith syndrome and Malan syndrome.

Published in:

International Journal of Developmental Neuroscience, 2023, v. 83, n. 5, p. 479, doi. 10.1002/jdn.10280

By:

Uzman, Ceren Yılmaz;
Gürsoy, Semra;
Hazan, Filiz

Publication type:

Article

Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants.

Published in:

Neurological Sciences, 2021, v. 42, n. 5, p. 2045, doi. 10.1007/s10072-020-04988-0

By:

Hazan, Filiz;
Gürsoy, Semra;
Unalp, Aycan;
Yılmaz, Unsal;
Demirağ, Bengü;
Aydin Köker, Sultan;
Ozyılmaz, Berk;
Erdogan, Kadri Murat;
Kalenderer, Önder;
Erkuş, Serkan;
Gürçınar, Müge;
Tükün, Ajlan

Publication type:

Article

AUDIOLOGICAL EVALUATION OF A 44-MONTH OLD CHILD WITH BURN-MCKEOWN SYNDROME:CASE REPORT.

Published in:

Journal of International Advanced Otology, 2015, v. 11, p. 81

By:

Kirkim, Gunay;
Kirazli, Gulce;
Hazan, Filiz;
Guneri, Enis Alpin

Publication type:

Article

HAX1 mutation positive children presenting with haemophagocytic lymphohistiocytosis.

Published in:

British Journal of Haematology, 2017, v. 177, n. 4, p. 597, doi. 10.1111/bjh.14574

By:

Karapınar, Tuba H.;
Yılmaz Karapinar, Deniz;
Oymak, Yeşim;
Ay, Yılmaz;
Demirağ, Bengü;
Aykut, Ayça;
Onay, Hüseyin;
Hazan, Filiz;
Aydınok, Yeşim;
Özkınay, Ferda;
Vergin, Canan

Publication type:

Article

Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel EFNB1 Gene Mutation.

Published in:

Molecular Syndromology, 2021, v. 12, n. 5, p. 269, doi. 10.1159/000515697

By:

Gürsoy, Semra;
Hazan, Filiz;
Öztürk, Tülay;
Çolak, Rüya;
Çalkavur, Şebnem

Publication type:

Article

Novel Ocular and Inner Ear Anomalies in a Patient with Myhre Syndrome.

Published in:

Molecular Syndromology, 2019, v. 10, n. 6, p. 339, doi. 10.1159/000504829

By:

Gürsoy, Semra;
Hazan, Filiz;
Öztürk, Tülay;
ateş, Halil

Publication type:

Article

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 7, p. 881, doi. 10.1038/ejhg.2013.263

By:

Jones, Gabriela E;
Ostergaard, Pia;
Moore, Anthony T;
Connell, Fiona C;
Williams, Denise;
Quarrell, Oliver;
Brady, Angela F;
Spier, Isabel;
Hazan, Filiz;
Moldovan, Oana;
Wieczorek, Dagmar;
Mikat, Barbara;
Petit, Florence;
Coubes, Christine;
Saul, Robert A;
Brice, Glen;
Gordon, Kristiana;
Jeffery, Steve;
Mortimer, Peter S;
Vasudevan, Pradeep C

Publication type:

Article

Genetic approach to the patient and the family: A Rett Syndrome case with p.R270X mutation in MECP2 gene.

Published in:

2013

By:

Hazan, Filiz;
Guzel, Orkide;
Celegen, Mehmet;
Tukun, Ajlan

Publication type:

Case Study

Combined use of genetic and immunohistochemical analysis is a critical step in differential diagnosis of sarcoglycanopathies.

Published in:

Journal of Dr. Behcet Uz Children's Hospital, 2017, v. 7, n. 3, p. 247, doi. 10.5222/buchd.2017.247

By:

DİNİZ, Gülden;
ÖZGÖNÜL, Figen;
UNALP, Aycan;
HAZAN, Filiz;
TÜRE, Sabiha;
AKHAN, Galip

Publication type:

Article

Sequence and Copy Number Analyses of HEXB Gene in Patients Affected by Sandhoff Disease: Functional Characterization of 9 Novel Sequence Variants.

Published in:

PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0041516

By:

Zampieri, Stefania;
Cattarossi, Silvia;
Ramirez, Ana Maria Oller;
Rosano, Camillo;
Lourenco, Charles Marques;
Passon, Nadia;
Moroni, Isabella;
Uziel, Graziella;
Pettinari, Antonella;
Stanzial, Franco;
Kremer, Raquel Dodelson de;
Azar, Nydia Beatriz;
Hazan, Filiz;
Filocamo, Mirella;
Bembi, Bruno;
Dardis, Andrea

Publication type:

Article

Clinical and Genetic Characteristics of Patients with Common and Rare Types of Congenital Adrenal Hyperplasia: Novel Variants in STAR and CYP17A1.

Published in:

Medical Bulletin of Sisli Etfal Hospital, 2022, v. 56, n. 2, p. 291, doi. 10.14744/SEMB.2021.28044

By:

Koprulu, Ozge;
Ozkan, Behzat;
Acar, Sezer;
Nalbantoglu, Ozlem;
Donmez, Beyhan Ozkaya;
Arslan, Gulcin;
Hazan, Filiz;
Gursoy, Semra

Publication type:

Article

A Neonatal Case of Infantile Malignant Osteopetrosis Presenting with Thrombocytopenia and Hypotonicity: A Novel Mutation in Chloride Voltage-Gated Channel 7 Gene.

Published in:

Medical Bulletin of Sisli Etfal Hospital, 2022, v. 56, n. 1, p. 161, doi. 10.14744/SEMB.2021.88964

By:

Al, Isik Odaman;
Oymak, Yesim;
Hazan, Filiz;
Gursoy, Semra;
Ozturk, Tulay;
Bag, Ozlem;
Gozmen, Salih;
Karakaya, Nurgul;
Karapinar, Tuba Hilkay

Publication type:

Article

Spectrum of Clinical Manifestations in Turkish Patients with Williams-Beuren Syndrome: A Monocentric Study.

Published in:

Journal of Pediatric Research, 2021, v. 8, n. 3, p. 297, doi. 10.4274/jpr.galenos.2021.10179

By:

Gürsoy, Semra;
Hazan, Filiz;
Zihni, Cüneyt;
Acar, Sezer;
Yılmazer, Murat Muhtar;
Meşe, Timur;
Özkan, Behzat

Publication type:

Article

Identification of two AMH gene variants in two unrelated patients with persistent Müllerian duct syndrome: one novel variant.

Published in:

Gynecological Endocrinology, 2021, v. 37, n. 5, p. 476, doi. 10.1080/09513590.2021.1908253

By:

Acar, Sezer;
Nalbantoğlu, Özlem;
Gürsoy, Semra;
Özkaya, Beyhan;
Köprülü, Özge;
Arslan, Gülçin;
Hazan, Filiz;
Özkan, Behzat

Publication type:

Article