Localization of the spherocytosis gene to chromosome segment 8p11.22----8p21

Autor:	M, Kitatani, H, Chiyo, M, Ozaki, S, Shike, S, Miwa
Rok vydání:	1988
Předmět:	Male Karyotyping Chromosome Mapping Humans Infant Spherocytosis Hereditary Chromosome Deletion Chromosome Banding Chromosomes Human Pair 8
Zdroj:	Human genetics. 78(1)
ISSN:	0340-6717
Popis:	A case of hereditary spherocytosis (HS) is reported. Cytogenetic study revealed a de novo minute deletion of chromosome 8. The critical portion which affected the expression of the HS phenotype appeared to be localized to 8p11.22----8p21.1.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::eaf52b59d25993a7f4f1576d1106e507 https://pubmed.ncbi.nlm.nih.gov/3338796 Zobrazit plný text záznamu Full text from SpringerLink