PDF) Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes
PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization
PDF) Turner's syndrome and pregnancy: Has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review
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
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
F R I D A Y • A P R I L - Pediatric Academic Societies
ΠΑΠΟΥΛΙΔΗΣ Ι. - PDF ΔΩΡΕΑΝ Λήψη
Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities | PNAS
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
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PDF) Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report
BALCANICA XXXIX - Балканолошки институт САНУ
ΑΔΕΙΟΔΟΤΗΜΕΝΟΙ ΔΙΑΜΕΣΟΛΑΒΗΤΕΣ ΜΕΤΕΓΓΡΑΦΩΝ ΠΟΔΟΣΦΑΙΡΙΣΤΩΝ ΑΠΟ ΤΗΝ Ε.Π.Ο. - 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
Molecular Research Papers - Academia.edu
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
PDF) Non-trophoblastic tumor of the placenta with combined histologic features of chorangioma and leiomyoma | Dimosthenis Miliaras, Ioannis Papoulidis, and Xeni Miliara - Academia.edu
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
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
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | PNAS
