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G Turanli

Showing results (11-20 of 14) with videos related to

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Genetic Counseling (Geneva, Switzerland)|September 12, 2018
A VERY RARE CAUSE OF APNEA IN THE NEONATAL PERIOD: JOUBERT SYNDROMEG Demirel, A Yilmaz, B Vatansever, et al.
Neuropediatrics|April 12, 2005
Congenital hydrocephalus as a rare association with ligneous conjunctivitis and type I plasminogen deficiencyA T Aslan, U Ozcelik, D Dogru, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 14, 1999
Rasmussen encephalitis in childhoodM Topçu, G Turanli, F M Aynaci, et al.
Journal of Intellectual Disability Research : JIDR|January 16, 2007
A multidisciplinary approach to the management of individuals with fragile X syndromeY Alanay, F Unal, G Turanli, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Genetic Counseling (Geneva, Switzerland)|September 12, 2018
A VERY RARE CAUSE OF APNEA IN THE NEONATAL PERIOD: JOUBERT SYNDROMEG Demirel, A Yilmaz, B Vatansever, et al.
Neuropediatrics|April 12, 2005
Congenital hydrocephalus as a rare association with ligneous conjunctivitis and type I plasminogen deficiencyA T Aslan, U Ozcelik, D Dogru, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 14, 1999
Rasmussen encephalitis in childhoodM Topçu, G Turanli, F M Aynaci, et al.
Journal of Intellectual Disability Research : JIDR|January 16, 2007
A multidisciplinary approach to the management of individuals with fragile X syndromeY Alanay, F Unal, G Turanli, et al.
Pageof 2