Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
PDF) Non-trophoblastic tumor of the placenta with combined histologic features of chorangioma and leiomyoma | Dimosthenis Miliaras, Ioannis Papoulidis, and Xeni Miliara - Academia.edu
F R I D A Y • A P R I L - Pediatric Academic Societies
BALCANICA XXXIX - Балканолошки институт САНУ
PDF) A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization
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 -
FISH analysis to confirm duplication. The analysis was performed using... | Download Scientific Diagram
OBM Genetics | Identification of a Small Supernumerary Marker Chromosome Involving 11p14.1q12.1 in a Prenatal Case: Clinical and Molecular Characterization
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Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | PNAS
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
PDF) Turner's syndrome and pregnancy: Has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review
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
The fetal karyotype; the arrow shows the duplicated chromosome 1. | Download Scientific Diagram
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
PDF) ONLINE PROPOSED GRADUATE PROGRAM ON GEOPOLITICS AND RELIGIOUS AND ECUMENICAL RELATIONS The Program | Spyridoula Athanasopoulou-Kypriou - Academia.edu
Molecular Research Papers - Academia.edu
PDF) Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing. - Abstract - Europe PMC
SCTS Bulletin Issue 07 by Open Box Media & Communications - Issuu
Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities | PNAS
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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) Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes
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
