Z. Yuksel

发表

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.

Kathryn Roeder, Liping Wei, Jeanselle Dea, 2014, Cell reports.

Asymmetric Posterior Thoracolumbar Fixation following a Posterolateral Transpedicular Approach for Unilateral Vertebral Disease

A. Karakaşlı, Z. Yuksel, M. Yılmaz, 2015, Neurologia medico-chirurgica.

Fahr's Syndrome: A Report of Two Cases

D. Tunçel, Z. Yuksel, 2007 .

A novel KIF7 mutation in two affected siblings with acrocallosal syndrome

T. Attié-Bitach, A. Ichkou, Z. Yuksel, 2015, Clinical dysmorphology.

A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing.

Tuck C. Ngun, E. Vilain, M. Fellous, 2016, Human reproduction.

Prevalence of Nonclassic Congenital Adrenal Hyperplasia in Turkish Children Presenting with Premature Pubarche, Hirsutism, or Oligomenorrhoea

S. Artan, Z. Yuksel, E. Şimşek, 2014, International journal of endocrinology.

De Novo Insertions and Dele tions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder Graphical

Jeffrey D. Mandell, Michael F. Walker, Michael J. DiCola, 2022 .

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.

J. Lupski, R. Gibbs, E. Boerwinkle, 2019, American journal of human genetics.

Early onset marfan syndrome: Atypical clinical presentation of two cases

N. Narin, A. Baykan, O. Pamukcu, 2015, Balkan journal of medical genetics : BJMG.

Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans

Stephan J Sanders, E. Grigorenko, S. Mane, 2014, European Journal of Human Genetics.

Multiple sclerosis and parkinsonism: a case report.

E. İdiman, Z. Yuksel, V. Ozturk, 2002, Functional neurology.