![Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases - Papoulidis - 2015 - Prenatal Diagnosis - Wiley Online Library Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases - Papoulidis - 2015 - Prenatal Diagnosis - Wiley Online Library](https://obgyn.onlinelibrary.wiley.com/cms/asset/4d235dcb-3758-49cf-b821-c02804f0785e/pd.v35.13.cover.jpg)
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases - Papoulidis - 2015 - Prenatal Diagnosis - Wiley Online Library
![Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library](https://obgyn.onlinelibrary.wiley.com/cms/asset/2d1ee835-2de4-42f4-9caf-5ca49cdaf14a/pd.2295.fp.png)
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library
![Distal 4p microdeletion in a case of Wolf‐Hirschhorn syndrome with congenital diaphragmatic hernia - Casaccia - 2006 - Birth Defects Research Part A: Clinical and Molecular Teratology - Wiley Online Library Distal 4p microdeletion in a case of Wolf‐Hirschhorn syndrome with congenital diaphragmatic hernia - Casaccia - 2006 - Birth Defects Research Part A: Clinical and Molecular Teratology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/44c4f0ae-2a80-4892-a78a-bbdb4f735600/mfig001.jpg)
Distal 4p microdeletion in a case of Wolf‐Hirschhorn syndrome with congenital diaphragmatic hernia - Casaccia - 2006 - Birth Defects Research Part A: Clinical and Molecular Teratology - Wiley Online Library
![Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6935954/bin/CG-20-226-f4.jpg)
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
![Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | PNAS Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | PNAS](https://www.pnas.org/content/105/51/20458/F1.large.jpg)
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | PNAS
![PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334-kb deletion: A case report PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334-kb deletion: A case report](https://i1.rgstatic.net/publication/258501920_Prenatal_detection_of_TAR_syndrome_in_a_fetus_with_compound_inheritance_of_an_RBM8A_SNP_and_a_334-kb_deletion_A_case_report/links/56af442f08ae28588c62f2cc/largepreview.png)
PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334-kb deletion: A case report
![Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | PNAS Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | PNAS](https://www.pnas.org/content/105/50/19920/F1.large.jpg)
Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | PNAS
![Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6935954/bin/CG-20-226-f2.jpg)
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
![PDF) ONLINE PROPOSED GRADUATE PROGRAM ON GEOPOLITICS AND RELIGIOUS AND ECUMENICAL RELATIONS The Program | Spyridoula Athanasopoulou-Kypriou - Academia.edu PDF) ONLINE PROPOSED GRADUATE PROGRAM ON GEOPOLITICS AND RELIGIOUS AND ECUMENICAL RELATIONS The Program | Spyridoula Athanasopoulou-Kypriou - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/64062485/mini_magick20200730-24096-sx6w4.png?1596178017)
PDF) ONLINE PROPOSED GRADUATE PROGRAM ON GEOPOLITICS AND RELIGIOUS AND ECUMENICAL RELATIONS The Program | Spyridoula Athanasopoulou-Kypriou - Academia.edu
![PDF) Turner's syndrome and pregnancy: Has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review PDF) Turner's syndrome and pregnancy: Has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review](https://i1.rgstatic.net/publication/47348765_Turner's_syndrome_and_pregnancy_Has_the_45X47XXX_mosaicism_a_different_prognosis_Own_clinical_experience_and_literature_review/links/56aba10908aeadd1bdce5a9e/largepreview.png)
PDF) Turner's syndrome and pregnancy: Has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review
![FISH analysis to confirm duplication. The analysis was performed using... | Download Scientific Diagram FISH analysis to confirm duplication. The analysis was performed using... | Download Scientific Diagram](https://i1.rgstatic.net/publication/261105701_Proximal_10q_duplication_in_a_child_with_severe_central_hypotonia_characterized_by_array-comparative_genomic_hybridization_A_case_report_and_review_of_the_literature/links/549ffb8e0cf267bdb8ff633c/largepreview.png)
FISH analysis to confirm duplication. The analysis was performed using... | Download Scientific Diagram
![PDF) Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications PDF) Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications](|https://0.academia-photos.com/attachment_thumbnails/40248463/mini_magick20190221-7723-1p14ss3.png?1550784793)
PDF) Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications
![PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization](https://i1.rgstatic.net/publication/318693657_A_Girl_with_10_Mb_Distal_Xp_Deletion_Arising_from_Maternal_Pericentric_Inversion_Clinical_Data_and_Molecular_Characterization/links/599d75b20f7e9b892bb3c88b/largepreview.png)
PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization
![PDF) Proximal 10q duplication in a child with severe central hypotonia characterized by array- comparative genomic hybridization: A case report and review of the literature | Orsetta Zuffardi - Academia.edu PDF) Proximal 10q duplication in a child with severe central hypotonia characterized by array- comparative genomic hybridization: A case report and review of the literature | Orsetta Zuffardi - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/41430941/mini_magick20190219-19608-1xsvn3p.png?1550590542)
PDF) Proximal 10q duplication in a child with severe central hypotonia characterized by array- comparative genomic hybridization: A case report and review of the literature | Orsetta Zuffardi - Academia.edu
![Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities | PNAS Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities | PNAS](https://www.pnas.org/content/103/36/13403/F1.large.jpg)
Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities | PNAS
![The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis - Toomes - 2003 - The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis - Toomes - 2003 -](https://onlinelibrary.wiley.com/cms/asset/b6014414-27fd-4ac3-a663-4ecd7d7b6f66/gcc.v59.12.cover.jpg)
The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis - Toomes - 2003 -
![Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6935954/bin/CG-20-226-f1.jpg)
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
![Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature - Sifakis - 2014 - Birth Defects Research Part Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature - Sifakis - 2014 - Birth Defects Research Part](https://onlinelibrary.wiley.com/cms/asset/b64bc0a6-f016-40f1-91c1-c22b4c88555f/bdra.v100.4.cover.jpg)