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Autor:
Konstantina Merou, Katherine Anagnostopoulou, Michael B. Petersen, Zeynep Tümer, Efi Pandelia, Yolanda Gyftodimou, Catherine Sarri, Haris Kontos, Sofia Douzgou, Elena Giouroukou, Katerina Papanikolaou, Gilbert B. Côté, Maria Grigoriadou, Haris Kokotas
Publikováno v:
Cytogenetic and Genome Research. 145:6-13
Côté et al. [1981] suggested that ring chromosomes with or without deletions share a common pattern of phenotypic anomalies, regardless of which chromosome is involved. The phenotype of this ‘general ring syndrome' consists of growth failure with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9ad97402ec40549b07dd3a3655ad579
https://doi.org/10.1159/000382046
https://doi.org/10.1159/000382046
