Personnel - ATG Genetics Laboratories
The fetal karyotype; the arrow shows the duplicated chromosome 1. | Download Scientific Diagram
PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report | Makarios Eleftheriades - Academia.edu
PDF) Turner's syndrome and pregnancy: Has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
PDF) Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334-kb deletion: A case report
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
PDF) Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes
Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | PNAS
PDF) Non-trophoblastic tumor of the placenta with combined histologic features of chorangioma and leiomyoma | Dimosthenis Miliaras, Ioannis Papoulidis, and Xeni Miliara - Academia.edu
Molecular Research Papers - Academia.edu
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
Pilot study of a novel multi‐functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single‐gene disorder screening - Luo - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library
FISH analysis to confirm duplication. The analysis was performed using... | Download Scientific Diagram
Α ΕΙΟ ΟΤΗΜΕΝΟΙ ΙΑΜΕΣΟΛΑΒΗΤΕΣ ΜΕΤΕΓΓΡΑΦΩΝ ΠΟ ΟΣΦΑΙΡΙΣΤΩΝ ΑΠΟ ΤΗΝ Ε.Π.Ο. - PDF Free Download
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
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
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
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 -
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Christian Brothers' High School Lewisham 2020 School Annual by CBHS Lewisham - Issuu
