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
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
Array‐CGH identifies the 334‐kb deletion in the long arm of chromosome... | Download Scientific Diagram
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
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
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - 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
PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Walter Cunningham Αδελφός Σαμουήλ papoulidis ioannis mail εργασία για το σπίτι Διαρκής Πλαστικότητα
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
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | PNAS
PDF) Α Case of Triplets Concordant for Schizophrenia: Psychopathological Considerations | George B Mitropoulos - Academia.edu
Trisomy 1 in an early pregnancy failure - Vičić - 2008 - 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
PDF) Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: 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
Annals REPORT ON THE ACTIVITIES OF THE INSTITUTE IN PDF Free Download
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
Walter Cunningham Αδελφός Σαμουήλ papoulidis ioannis mail εργασία για το σπίτι Διαρκής Πλαστικότητα
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
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
Alignment of the cDNA sequences for human trabeculin-and-, limited to... | Download Scientific Diagram
PDF) Tetrasomy 9p Mosaicism Associated with a Normal Phenotype in Two Cases
