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Journal of Pediatric Hematology/Oncology|March 3, 2011
WAGR syndrome with tetralogy of Fallot and hydrocephalusHaci Ahmet Demir, Ali Varan, Eda G Utine, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 23, 2012
Bilateral anterior segment dysgenesis in an infant with partial trisomy 16q and partial monosomy 3pOzlem Dikmetas, Pelin Ozlem Simsek Kiper, Mehmet C Mocan, et al.
European Journal of Medical Genetics|April 29, 2008
Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGHEda G Utine, Yasemin Alanay, Dilek Aktas, et al.
American Journal of Medical Genetics. Part A|October 9, 2017
Homozygous indel mutation in CDH11 as the probable cause of Elsahy-Waters syndromeEkim Z Taskiran, Beren Karaosmanoglu, Can Koşukcu, et al.
Molecular Cytogenetics|June 1, 2010
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pairDilek Aktas, Eda G Utine, Kristin Mrasek, et al.
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