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Author
7
Syrrou, M.
4
Fryns, J. P.
3
Sofikitis, N.
2
Kaponis, A.
2
Kitsos, G.
2
Lagae, L.
2
Lolis, D.
2
Loutradis, D.
2
Mio, Y.
2
Miyagawa, I.
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18
Humans
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Female
10
In Situ Hybridization, Fluorescence
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Child, Preschool
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18
journalArticle
Date
1
2010 - 2011
11
2000 - 2009
6
1997 - 1999
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
Σχολή Επιστημών Υγείας
Τμήμα Ιατρικής
Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Results 1-10 of 18 (Search time: 0.078 seconds).
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Refractory photosensitive epilepsy associated with a complex rearrangement of chromosome 2 (Journal article)
R831X mutation of the androgen receptor gene in an adolescent with complete androgen insensitivity syndrome and bilateral testicular hamartomata (Journal article)
Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter) (Journal article)
Xp22.3; Yq11.2 chromosome translocation and its clinical manifestations (Journal article)
Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation (Journal article)
Use of a highly sensitive quantitative telomerase assay in intracytoplasmic sperm injection programmes for the treatment of 47,XXY non-mosaic Klinefelter men (Journal article)
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter (Journal article)
Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delay (Journal article)
Infertility and multiple urogenital abnormalities in a male with mosaic 46,XY/45,XO/47,XXY karyotype and mixed phenotype (Journal article)
Mosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infant (Journal article)