المؤلفون: Jean-Pierre Fryns, Heike Starke, Mariluce Riegel, Natalia Rumyantseva, Vladimir Trifnov, Albert Schinzel, Cindy Melotte, I Salden, Joris Vermeesch, Thomas Liehr, Irina Naumchik, A Polityko, Gert Matthijs

المصدر: European journal of medical genetics. 48(3)

مصطلحات موضوعية: Genetic Markers, Neocentromere, Isochromosome, Biology, Craniofacial Abnormalities, Pallister–Killian syndrome, Ulnar–mammary syndrome, Intellectual Disability, Genetics, medicine, Humans, Abnormalities, Multiple, Child, Small supernumerary marker chromosome, Genetics (clinical), In Situ Hybridization, Fluorescence, Oligonucleotide Array Sequence Analysis, Chromosomes, Human, Pair 12, General Medicine, Syndrome, Chromosome microdissection, medicine.disease, Aneuploidy, Molecular biology, Phenotype, Genetic marker, Tetrasomy, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::265c57adc060d7302bb7210e0365b58b
https://pubmed.ncbi.nlm.nih.gov/16179227