A. Ulgenalp

发表

Congenital cardiac defects with 22q11 deletion.

T. Meşe, E. Bora, D. Erçal, 2003, The Turkish journal of pediatrics.

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

A. Caglayan, O. Ozdemır, S. Artan, 2022, Functional & Integrative Genomics.

The effects of epigenetic regulation on phenotypic expressivity in Turkish patients with familial Mediterranean fever

G. Bozkaya, A. Soylu, S. Kavukçu, 2019, Indian Journal of Rheumatology.

The association of beta-fibrinogen 455 G/A gene polymorphism with left atrial thrombus and severe spontaneous echo contrast in atrial fibrillation.

N. Barış, B. Akdeniz, Omer Senarslan, 2010, Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology.

Relationship between plasminogen activator inhibitor‐1 gene alterations and fibrosis in peritoneal dialysis patients

E. Ataman, M. Tanrisev, S. Ersan, 2020, Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy.

Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation sequencing panel and MLPA analysis in Turkey.

A. Caglayan, S. Saydam, A. Sevinc, 2022, Cancer genetics.

Protracted febrile myalgia syndrome in a patient with familial Mediterranean fever homozygous for the E148Q mutation.

N. Uzuner, A. Soylu, S. Kavukçu, 2008, Seminars in arthritis and rheumatism.

Long‐standing fever and Angelman syndrome: Report of two cases

U. Yiş, S. Kurul, E. Dirik, 2008, Journal of paediatrics and child health.

PDFlib PLOP: PDF Linearization, Optimization, Protection Page inserted by evaluation version

U. Yiş, S. Kurul, E. Dirik, 2008 .

Lack of Association of Childhood Partial Epilepsy with Brain Derived Neurotrophic Factor Gene

E. Bora, A. Ulgenalp, A. Unalp, 2012, TheScientificWorldJournal.

Role of apolipoprotein E in febrile convulsion.

E. Bora, O. Giray, A. Ulgenalp, 2008, Pediatric neurology.

Serum motilin levels and motilin gene polymorphisms in children with functional constipation.

N. Arslan, Emel Ulusoy, T. Kume, 2016, Minerva pediatrica.

Three novel mutations of CHD7 gene in two turkish patients with charge syndrome; A double point mutation and an insertion

E. Ataman, S. Gürsoy, A. Ulgenalp, 2015, Balkan journal of medical genetics : BJMG.

A 12-Year-Old Girl with Bilateral Coats Disease and ABCA4 Gene Mutation

A. Yaman, E. Bora, S. Kavukçu, 2018, Case Reports in Ophthalmology.

Lymphoid tissue histology in a patient with ICF syndrome.

E. Bora, B. Makay, A. Ulgenalp, 2012, Journal of investigational allergology & clinical immunology.

An unusual case of monosomy 18p: minor malformations with speech delay.

H. Ozkan, E. Bora, O. Giray, 2005, The Turkish journal of pediatrics.

Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.

H. Karasoy, S. Kurul, E. Dirik, 2004, The Turkish journal of pediatrics.

Prolonged unconjugated hyperbilirubinaemia associated with the haem oxygenase‐1 gene promoter polymorphism

H. Ozkan, A. Kumral, N. Duman, 2010, Acta paediatrica.

MIRAGE syndrome in a 10-year-old girl with a novel Lys1024Glu missense variant in SAMD9.

A. Caglayan, S. Asilsoy, S. Gürsoy, 2023, Clinical dysmorphology.

Unexpected finding in kidney biopsy of a child with nephrotic proteinuria: Answers

A. Caglayan, Gizem Yıldız, A. Soylu, 2022, Pediatric Nephrology.

Clinical Heterogeneity in Patients with Long QT Syndrome and Segregation of Single Nucleotide Variants and Clinical Symptoms in 17 Affected Families

E. Bora, E. E. Ozcan, A. Ulgenalp, 2023, Molecular Syndromology.

Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patients.

U. Yiş, E. Bora, A. Ulgenalp, 2024, Neurogenetics.