Emmanouil Manolakos

Emmanouil Manolakos

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Emmanouil Manolakos

Emmanouil Manolakos

Publications by authors named "Emmanouil Manolakos"

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Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study.

Prenat Diagn 2017 Jun 23;37(6):583-592. Epub 2017 May 23.

Third Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, Thessaloniki, Greece.

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http://dx.doi.org/10.1002/pd.5051DOI Listing
June 2017

Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male.

Mol Cytogenet 2015 17;8:71. Epub 2015 Sep 17.

Access to genome P.C., Clinical Laboratory Genetics, 33A Ethn. Antistaseos str, 55134 Thessaloniki, Greece ; Department of Medical Genetics, University of Cagliari, Binaghi Hospital, Cagliari, Italy.

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http://www.molecularcytogenetics.org/content/8/1/71
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http://dx.doi.org/10.1186/s13039-015-0175-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574176PMC
September 2015

A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics.

Mol Cytogenet 2014 3;7(1):92. Epub 2014 Dec 3.

Eurogenetica S.A., Laboratory of Genetics, Michalakopoulou 125& Vervainon 14, 11527 Athens, Thessaloniki Greece ; Department of Medical Genetics, University of Cagliari, Binaghi Hospital, Cagliari, Italy.

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http://dx.doi.org/10.1186/s13039-014-0092-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265435PMC
December 2014

De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features.

Meta Gene 2014 Dec 15;2:274-82. Epub 2014 Apr 15.

Eurogenetica S.A., Laboratory of Genetics, Athens-Thessaloniki, Greece ; Cattedra di Genetica Medica, Ospedale Binaghi, Cagliari, Italy.

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http://dx.doi.org/10.1016/j.mgene.2014.03.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287824PMC
December 2014

Sonographic antenatal diagnosis of congenital dacryocystoceles.

J Clin Ultrasound 2012 Jul-Aug;40(6):375-7. Epub 2012 May 19.

Department of Clinical Embryology, Larissa Medical School, University of Thessaly, Larisa, Greece.

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http://dx.doi.org/10.1002/jcu.21937DOI Listing
October 2012

Uterine arteriovenous malformations induced after diagnostic curettage: a systematic review.

Arch Gynecol Obstet 2011 Nov 9;284(5):1137-51. Epub 2011 Sep 9.

Department of Obstetrics and Gynaecology, Royal Free Hospital, University College Pond Street, NW3 2Q London, UK.

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http://dx.doi.org/10.1007/s00404-011-2067-7DOI Listing
November 2011

Common structural features characterize interstitial intrachromosomal Xp and 18q triplications.

Am J Med Genet A 2011 Nov 30;155A(11):2681-7. Epub 2011 Sep 30.

Istituto Scientifico E. Medea, Bosisio Parini (LC), Italy.

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http://dx.doi.org/10.1002/ajmg.a.34248DOI Listing
November 2011