Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Συντάκτης Τίτλος Τύπος [ Έτος] Φίλτρα: Keyword is Comparative Genomic Hybridization [Clear All Filters]
De novo Unbalanced 1;22 Translocation with 22q11 Deletion Syndrome..
Cytogenet Genome Res. 158(1), 32-37.
(2019). Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature..
Cytogenet Genome Res. 159(3), 109-118.
(2019). Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly..
Pediatr Res. 82(2), 253-260.
(2017).
(2017). Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties..
Cytogenet Genome Res. 147(2-3), 118-23.
(2015). Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay..
Cytogenet Genome Res. 145(1), 19-24.
(2015). Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome..
Am J Med Genet A. 164A(3), 764-8.
(2014). A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth..
Prenat Diagn. 30(6), 586-8.
(2010).