Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array‐CGH - Manolakos - 2009 - 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
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
Molecular Research Papers - Academia.edu
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | PNAS
F R I D A Y • A P R I L - Pediatric Academic Societies
PDF) Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report
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) An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review | Emmanouil Manolakos and Thomas Liehr - Academia.edu
The fetal karyotype; the arrow shows the duplicated chromosome 1. | Download Scientific Diagram
Christian Brothers' High School Lewisham 2020 School Annual by CBHS Lewisham - Issuu
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
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 -
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
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
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
Α ΕΙΟ ΟΤΗΜΕΝΟΙ ΙΑΜΕΣΟΛΑΒΗΤΕΣ ΜΕΤΕΓΓΡΑΦΩΝ ΠΟ ΟΣΦΑΙΡΙΣΤΩΝ ΑΠΟ ΤΗΝ Ε.Π.Ο. - PDF Free Download
SCTS Bulletin Issue 07 by Open Box Media & Communications - Issuu
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
BALCANICA XXXIX - Балканолошки институт САНУ
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
