Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Danai, Stambouli"'
Autor:
George Koumbaris, Achilleas Achilleos, Michalis Nicolaou, Charalambos Loizides, Kyriakos Tsangaras, Elena Kypri, Petros Mina, Carolina Sismani, Voula Velissariou, Georgia Christopoulou, Pantelis Constantoulakis, Emmanouil Manolakos, Ioannis Papoulidis, Danai Stambouli, Marios Ioannides, Philippos Patsalis
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-9 (2019)
Abstract Background Non-invasive prenatal testing (NIPT) has been widely adopted for the detection of fetal aneuploidies and microdeletion syndromes, nevertheless, limited clinical utilization has been reported for the non-invasive prenatal screening
Externí odkaz:
https://doaj.org/article/c8dd64cfe8c54040bbd618666302dd47
Autor:
Adrian Preda, C Gîngu, Danai Stambouli, Catalin Baston, Anca Pavel, Gabriela Anton, Ismail Gener
Publikováno v:
Romanian Biotechnological Letters. 24:1043-1049
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5cc01dd692c48e9a908fe85c5946ea
https://doi.org/10.25083/rbl/24.6/1043.1049
https://doi.org/10.25083/rbl/24.6/1043.1049
Autor:
Simona Sosoi, Dan Ruican, Ioana Streata, Anda Ungureanu, Gabriela Popescu‑Hobeanu, Luiza Dimoş, Florin Burada, Danai Stambouli, Ioana Florina Mihai, Dominic Gabriel Iliescu, Rodica Daniela Nagy
Publikováno v:
Experimental and Therapeutic Medicine
Distal trisomy or duplication of 15q is a very rare chromosomal disorder; most of the previously reported cases were derived from unbalanced translocations involving chromosome 15 and another chromosome, whereas other mechanisms (e.g. duplication) ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1798affc0cf1eae277420edbf2a7843
https://doi.org/10.3892/etm.2021.9735
https://doi.org/10.3892/etm.2021.9735
Autor:
Elena Kypri, Voula Velissariou, Carolina Sismani, Danai Stambouli, Emmanouil Manolakos, Pantelis Constantoulakis, Philippos C. Patsalis, Michalis Nicolaou, Marios Ioannides, Kyriakos Tsangaras, Georgia Christopoulou, Ioannis Papoulidis, Achilleas Achilleos, George Koumbaris, Petros Mina, Charalambos Loizides
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-9 (2019)
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-9 (2019)
Background Non-invasive prenatal testing (NIPT) has been widely adopted for the detection of fetal aneuploidies and microdeletion syndromes, nevertheless, limited clinical utilization has been reported for the non-invasive prenatal screening of monog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e543c3c5dd3f7292dbfca18dbfb8b0
Publikováno v:
Medic.ro. 1:13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbfd756c7c605b1c6ac0142b70b94a58
https://doi.org/10.26416/med.121.1.2018.1522
https://doi.org/10.26416/med.121.1.2018.1522
Autor:
Cosmina-Raluca Costache, Oana Popa, Danai Stambouli, Mariana-Cristina Costache-Outas, Madalina-Aura Vintila, Camelia Procopiuc
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15fcdeca3156fce1f6f30c2b2c6c52ad
https://doi.org/10.1530/endoabs.38.p374
https://doi.org/10.1530/endoabs.38.p374
Autor:
Vasiliki, Chini, Danai, Stambouli, Florina Mihaela, Nedelea, George Alexandru, Filipescu, Diana, Mina, Marios, Kambouris, Hatem, El-Shantil
Publikováno v:
Eye science. 29(2)
Prenatal diagnosis was requested for an undiagnosed eye disease showing X-linked inheritance in a family. No medical records existed for the affected family members. Mapping of the X chromosome and candidate gene mutation screening identified a c.C26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b80beaf8c79b7c37a49ec4ee3979af53
https://pubmed.ncbi.nlm.nih.gov/26011961
https://pubmed.ncbi.nlm.nih.gov/26011961
Autor:
Hatem El-Shanti, Danai Stambouli, Florina M ihaela Nedelea, Marios Kambouris, George A lexandru Filipescu, V. Chini, Diana Mina
Publikováno v:
Qatar Foundation Annual Research Forum Volume 2012 Issue 1.
Background and Objectives: A pregnant female requested prenatal diagnosis for a congenital and complex eye disease segregating in her family. The three-generation pedigree of Romanian ethnic origin was suggestive of an X-linked inheritance, due to ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4cea2135fb16d0a5e6e25594cc862f0
https://doi.org/10.5339/qfarf.2012.bmp49
https://doi.org/10.5339/qfarf.2012.bmp49