S. Berker-Karauzum

Turner Syndrome with Isochromosome Xq and Familial Reciprocal Translocation t(4;16)(p15.2;p13.1)

G. Luleci, B. Karaman, S. Yakut, 2011, Balkan journal of medical genetics : BJMG.

Multidirectional and simultaneous evaluation of gastroschisis-related intestinal damage in chick embryos.

N. Demir, Duygu Yasar, M. Melikoglu, 2014, Journal of pediatric surgery.

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.

G. Luleci, S. Yakut, Z. Çetin, 2011, Genetic counseling.

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).

V. Sheffield, S. Jacobson, A. Fulton, 2003, American journal of human genetics.

UvA-DARE ( Digital Academic Repository ) Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus ( BBS 1 )

V. Sheffield, S. Jacobson, A. Fulton, 2003 .

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Christian R Marshall, Alexandre Reymond, Paige Kaplan, 2008, American journal of human genetics.

Array comparative genomic hybridization analysis of adult acute leukemia patients.

G. Luleci, Duygu Yasar, G. Toruner, 2010, Cancer genetics and cytogenetics.

Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism

G. Luleci, M. Parlak, Z. Çetin, 2013, European Journal of Pediatrics.

A case with de novo interstitial deletion of chromosome 7q21.1-q22.

A. Baumer, G. Lüleci, A. Schinzel, 2005, Genetic Counseling.