Elif Yosunkaya-Fenerci
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 9 publications
A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication.
Journal: Gene
Published: March 08, 2013
Circumferential skin folds and multiple anomalies: confirmation of a distinct autosomal recessive Michelin tire baby syndrome.
Journal: Clinical dysmorphology
Published: January 18, 2013
A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia.
Journal: Clinical dysmorphology
Published: November 22, 2012
The very rare aglossia adactylia syndrome with a novel finding of mental retardation.
Journal: Genetic counseling (Geneva, Switzerland)
Published: May 23, 2012
Sudden vision loss in a mucopolysaccharidosis I patient receiving enzyme replacement therapy.
Journal: Genetic counseling (Geneva, Switzerland)
Published: February 07, 2012
Glioma risk associates with polymorphisms of DNA repair genes, XRCC1 and PARP1.
Journal: British journal of neurosurgery
Published: September 28, 2010
Rheumatoid arthritis risk associates with DNA repair gene XRCC1 Arg399Gln polymorphism in Turkish patients.
Journal: Rheumatology international
Published: June 18, 2010
Marked improvement in Segawa syndrome after L-dopa and selegiline treatment.
Journal: Pediatric neurology
Published: August 27, 2009
Supernumerary chromosome der(22)t(11;22): Emanuel syndrome associates with novel features.
Journal: Genetic counseling (Geneva, Switzerland)
Published: February 22, 2008
Showing 1-9 of 9
Last Updated: 09/26/2026