Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature

التفاصيل البيبلوغرافية
العنوان: Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature
المؤلفون: Isabella Mammi, Diana Postorivo, Aminta Varricchio, Maria Garzo, Elisa Nalesso, Teresa Mattina, Ilaria Catusi, Maria Paola Recalcati, Laura Cardarelli, Nicola Beltrami, Anna Sajeva, Maria Teresa Bonati, Daniela Giardino, Annapia Verri, Lidia Larizza, Asia Costa, Nicoletta Villa, Anna Maria Nardone
المصدر: European Journal of Medical Genetics. 61:173-180
بيانات النشر: Elsevier BV, 2018.
سنة النشر: 2018
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Gestational Age, 030105 genetics & heredity, Biology, Molecular cytogenetics, 03 medical and health sciences, Fetus, Chromosome 19, Genetics, medicine, Humans, Abnormalities, Multiple, Supernumerary, Copy-number variation, Small supernumerary marker chromosome, Genetic Association Studies, Genetics (clinical), Chromosome Aberrations, Mosaicism, Cytogenetics, Chromosome, General Medicine, Phenotype, Child, Preschool, Cytogenetic Analysis, Female, Chromosomes, Human, Pair 19
الوصف: Only a few subjects carrying supernumerary marker chromosomes derived from 19 chromosome (sSMC(19)) have been described to date and for a small portion of them the genic content has been defined at the molecular level. We present seven new different sSMCs(19) identified in eight individuals, seven of whom unrelated. The presence of the sSMC is associated with a clinical phenotype in five subjects, while the other three carriers, two of whom related, are normal. All sSMCs(19) have been characterized by means of conventional and molecular cytogenetics. We compare the sSMCs(19) carriers with a clinical phenotype to already described patients with gains (sSMCs or microduplications) of overlapping genomic regions with the aim to deepen the pathogenicity of the encountered imbalances and to assess the role of the involved genes on the phenotype. The present work supports the correlation between the gain of some chromosome 19 critical regions and specific phenotypes.
تدمد: 1769-7212
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee44c49bf4aa6e1d6440e91216290a5Test
https://doi.org/10.1016/j.ejmg.2017.11.007Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....1ee44c49bf4aa6e1d6440e91216290a5
قاعدة البيانات: OpenAIRE