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
Deletion 2q31.2‐q31.3 in a 4‐year‐old girl with microcephaly and severe mental retardation - Manolakos - 2011 - American Journal of Medical Genetics Part A - Wiley Online Library
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
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
PDF) Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
G-banding karyotype of the patient. It is illustrated the interstitial... | Download Scientific Diagram
Walter Cunningham Αδελφός Σαμουήλ papoulidis ioannis mail εργασία για το σπίτι Διαρκής Πλαστικότητα
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
PDF) The role of ascorbic acid in the prevention of atrial fibrillation after elective on-pump myocardial revascularization surgery: A single-center experience - a pilot study
The fetal karyotype; the arrow shows the duplicated chromosome 1. | Download Scientific Diagram
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
Walter Cunningham Αδελφός Σαμουήλ papoulidis ioannis mail εργασία για το σπίτι Διαρκής Πλαστικότητα
Array‐CGH identifies the 334‐kb deletion in the long arm of chromosome... | Download Scientific Diagram
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
F R I D A Y • A P R I L - Pediatric Academic Societies
Walter Cunningham Αδελφός Σαμουήλ papoulidis ioannis mail εργασία για το σπίτι Διαρκής Πλαστικότητα
Personnel - ATG Genetics Laboratories
Applicability of first‐trimester combined screening for fetal trisomy 21 in a resource‐limited setting in mainland China - Li - 2016 - BJOG: An International Journal of Obstetrics & Gynaecology - Wiley Online Library
PDF) A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth | Ioannis Papoulidis, O. Zuffardi, A. Athanasiadis, Elisavet Siomou, and Emanouil Manolakos - Academia.edu
PDF) Parental origin of mutations in sporadic case of Treacher Collins syndrome
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - Prenatal Diagnosis - Wiley Online Library
