Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Markos Mihalatos"'
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Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report
Autor: Sandro Orru, George Kitsos, Markos Mihalatos, Emmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, Rozita Neroutsou, Anja Weise, Haris Kokotas, Thomas Liehr, Michael B. Petersen
Publikováno v: Molecular Cytogenetics, Vol 1, Iss 1, p 24 (2008)
Molecular Cytogenetics
We report on a 7 years and 4 months old Greek boy with mild microcephaly and dysmorphic facial features. He was a sociable child with maxillary hypoplasia, epicanthal folds, upslanting palpebral fissures with long eyelashes, and hypertelorism. His ea
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df03ba2ef250d5a6cfc302f43ffd5377
https://doi.org/10.1186/1755-8166-1-24
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3
Evaluation of dHPLC in mutation screening of the APC gene in a Greek FAP cohort
Autor: Markos, Mihalatos, Angela, Apessos, John K, Triantafillidis, Paris A, Kosmidis, George, Fountzilas, Niki J, Agnantis, Drakoulis, Yannoukakos, George, Nasioulas
Publikováno v: Anticancer research. 23(3B)
Germline mutations in the APC gene predispose to colorectal adenomas leading to cancer in over 80% of patients. A multitude of mutations, dispersed throughout the gene, have been described. We wanted to evaluate the usefulness of denaturing high perf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::77650185cd264a81fde6f66241140469
https://pubmed.ncbi.nlm.nih.gov/12894559
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6
Akademický článek
Deep sequencing of a candidate region harboring the SOX9 gene for the canine XX disorder of sex development.
Autor: Nowacka‐Woszuk, J.1, Szczerbal, I.1, Pausch, H.2, Hundi, S.3, Hytönen, M. K.3, Grzemski, A.1, Flisikowski, K.4, Lohi, H.3, Switonski, M.1 switonsk@up.poznan.pl, Szydlowski, M.1 maciej@up.poznan.pl
Publikováno v: Animal Genetics. Jun2017, Vol. 48 Issue 3, p330-337. 8p.
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7
Akademický článek
Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients.
Autor: Mihalatos, Markos1 m.mihalat@hygeia.gr, Apessos, Angela1 a.apessos@hygeia.gr, Dauwerse, Hans2 h.dauwerse@lumc.nl, Velissariou, Voula3 voulavel@mitera.gr, Psychias, Aristidis4 a-psychias@otenet.gr, Koliopanos, Alexander5 alexcol@teledomenet.gr, Petropoulos, Konstantinos6, Triantafillidis, John K.7 jkt@panafonet.gr, Danielidis, Ioannis8 iodaniel@hol.gr, Fountzilas, George9 fountzil@med.auth.gr, Agnantis, Niki J.10 nagnanti@cc.uoi.gr, Nasioulas, Georgios1 g.nasioul@hygeia.gr
Publikováno v: BMC Cancer. 2005, Vol. 5, p40-8. 8p. 1 Chart, 1 Graph.
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8
Akademický článek
Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer.
Autor: Belogianni, Ioulia1 Iolia.Beloyianni@hygeia.gr, Apessos, Angela1 a.apessos@hygeia.gr, Mihalatos, Markos1 m.mihalat@hygeia.gr, Razi, Evangelia2 e.razis@hygeia.gr, Labropoulos, Stefanos2 slabropoulos@yahoo.com, Petounis, Andreas2 a.petouni@hygeia.gr, Gaki, Vasiliki3 zervosk@otenet.gr, Keramopoulos, Antonios3 g-vourli@hotmail.gr, Pandis, Nikos4 nikos.pandis@medgen.ath.forthnet.gr, Kyriacou, Kyriacos5 kyriacos@cing.ac.cy, Hadjisavvas, Andreas5 kyriacos@cing.ac.cy, Kosmidis, Paris6 parkosmi@otenet.gr, Yannoukakos, Drakoulis7 yannouka@rrp.demokritos.gr, Nasioulas, Georgios1 g.nasioul@hygeia.gr
Publikováno v: BMC Cancer. 2004, Vol. 4, p1-8. 8p. 1 Diagram, 2 Charts.
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