A patient with constitutional ring 1 chromosome characterized by SNP array CGH

التفاصيل البيبلوغرافية
العنوان: A patient with constitutional ring 1 chromosome characterized by SNP array CGH
المؤلفون: Sheila Saliganan, Joanna Lee, Sainan Wei
المصدر: Clinical Case Reports
بيانات النشر: Wiley, 2016.
سنة النشر: 2016
مصطلحات موضوعية: ring syndrome, 0301 basic medicine, Microcephaly, medicine.medical_specialty, dwarfism, growth retardation, Case Report, Case Reports, Biology, Ring (chemistry), ring 1 chromosome, cytogenetics, 03 medical and health sciences, Chromosome (genetic algorithm), medicine, microcephaly, chromosome 1, Genetics, Cytogenetics, General Medicine, Microdeletion syndrome, medicine.disease, 1q43q44 deletion, 030104 developmental biology, intellectual disability, array comparative genomic hybridization, Chromosome 21, Comparative genomic hybridization, SNP array
الوصف: Key Clinical Message We present a male patient with constitutional ring 1 chromosome and subsequent 6 Mb deletion at 1q43q44. The patient displays overlapping clinical features with reported patients with ring 1 chromosome and 1q43q44 microdeletion syndrome. To our knowledge, this is the first patient with ring 1 chromosome characterized by comparative genomic hybridization.
تدمد: 2050-0904
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::292fbef107c85fd95d98ddd4af26e42aTest
https://doi.org/10.1002/ccr3.522Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....292fbef107c85fd95d98ddd4af26e42a
قاعدة البيانات: OpenAIRE