Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 9 results:
Author Title Type [ Year] Filters: Keyword is Chromosome Deletion [Clear All Filters]
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). 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).
(2015). Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome..
Am J Med Genet A. 164A(3), 764-8.
(2014). An infant with ethylmalonic encephalopathy masquerading as a hematologic disorder..
J Child Neurol. 28(5), 668-71.
(2013).
(2013). Alleviation of myelodysplastic syndrome-associated skin rush after treatment with decitabine..
Eur J Haematol. 81(6), 489-90.
(2008). Genetic and epigenetic risks of intracytoplasmic sperm injection method..
Asian J Androl. 8(6), 643-73.
(2006).