Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Eleni, Sekerli"'
Autor:
Kosmas Sarafidis, Nikolaos Peroulis, Antonios Psarakis, Thomas Kataras, Eleni Tsoulou-Panidou, Anastasios Xefteris, Georgios Daskalakis, Eleni Sekerli, Aggeliki Malamidou, Eirini Oikonomidou, Eleni Agakidou, Sofia Charisiou, Georgios Efstathiou, Antonia Arampatzi
Publikováno v:
Cytogenetic and Genome Research. 159:109-118
In the present study, we report a case of a female infant with a de novo unbalanced t(14;15) translocation resulting in a 14-Mb deletion of the 15q11.1q14 region. The deletion includes the 15q11.2q13 Prader-Willi syndrome (PWS) critical region, while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d8fa8307ce0d7942e0151b29684b89c
https://doi.org/10.1159/000504159
https://doi.org/10.1159/000504159
Autor:
Georgia Vassiliou, Dimitrios Iliopoulos, Augerinos Topalidis, Despina Dimopoulou, Aikaterini Koutra, Eleni Sekerli, Alexandra Drakaki, Nikolaos Voyiatzis
Publikováno v:
Journal of Pediatric Neurology. :205-209
The family of extra structurally abnormal chromosomes includes supernumerary small chromosomes, which are related to developmental abnormalities. The most common supernumerary index chromosome is inverted duplicated chromosome 15. Two cytogenetic typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80f37b8a04a60df514448a17ef8cd118
https://doi.org/10.3233/jpn-2010-0390
https://doi.org/10.3233/jpn-2010-0390
Autor:
M Varras, Anastasios Xefteris, Anastasia Konstantinidou, Fani-Niki Varra, Viktoria-Konstantina Varra, Stella Akrivi, Antonia Arampatzi, Antonios Kondylios, Eleni Sekerli, Apostolos Fasoulopoulos
Publikováno v:
Journal of Molecular and Clinical Medicine. 3:19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3b0d27c39b559bb0c5b4aef50b2da09
https://doi.org/10.31083/j.jmcm.2020.01.001
https://doi.org/10.31083/j.jmcm.2020.01.001
Autor:
Eleni, Sekerli1 elenisekerli@yahoo.gr, Dimitrios, Katsanidis1, Vaya, Papadopoulou1, Areti, Makedou1, Norma, Vavatsi2, Mgadalini, Gatzola1
Publikováno v:
Journal of Genetics. Apr2008, Vol. 87 Issue 1, p91-93. 3p. 1 Chart.
Autor:
Dimitrios, Iliopoulos, Georgia, Vassiliou, Eleni, Sekerli, Vasiliki, Sidiropoulou, Alexandra, Tsiga, Despina, Dimopoulou, Nikolaos, Voyiatzis
Publikováno v:
Genetics and molecular research : GMR. 4(4)
The live birth of a triploidy infant is a very rare event and death usually occurs within the first hours of life. Triploid cases with a survival of more than two months are infrequent. We report on an infant with a 69,XXX chromosome constitution who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0dd2c0c64300fd59ea29f9c9a7d8101
https://pubmed.ncbi.nlm.nih.gov/16475122
https://pubmed.ncbi.nlm.nih.gov/16475122
Autor:
Eleni Sekerli, Nikolaos Voyiatzis, Dimitrios Iliopoulos, Vasiliki Sidiropoulou, Augerinos Topalidis, Despina Dimopoulou, Georgia Vassiliou
Publikováno v:
American journal of medical genetics. Part A. 140(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06efb014e5147b8e466ab27c4ebd1cb1
https://pubmed.ncbi.nlm.nih.gov/16333832
https://pubmed.ncbi.nlm.nih.gov/16333832