Guven Luleci
Antalya, Turkey
Last Updated: 09/26/2026
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Found 19 publications
Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia.
Journal: Molecular cytogenetics
Published: September 02, 2017
Chromosome abnormalities identified in 457 spontaneous abortions and their histopathological findings.
Journal: Turk patoloji dergisi
Published: May 07, 2015
Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases.
Journal: Turk patoloji dergisi
Published: October 11, 2014
Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma.
Journal: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica
Published: February 13, 2014
Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation.
Journal: The journal of obstetrics and gynaecology research
Published: February 12, 2014
The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation.
Journal: The Turkish journal of pediatrics
Published: January 03, 2014
Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
Journal: Pediatric neurology
Published: October 09, 2013
Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.
Journal: European journal of pediatrics
Published: March 04, 2013
Pulmonary alveolar microlithiasis with homozygous c.316G > C (p.G106R) mutation: a case report.
Journal: Turk patoloji dergisi
Published: September 27, 2012
Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).
Journal: Genetic counseling (Geneva, Switzerland)
Published: August 11, 2012
Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
Journal: Genetic counseling (Geneva, Switzerland)
Published: August 11, 2012
Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.
Journal: Gene
Published: July 13, 2012
Last Updated: 09/26/2026