Autor:	Jan‐Erik Niléhn, Inga Marie Nilsson
Rok vydání:	1962
Předmět:	congenital hereditary and neonatal diseases and abnormalities Pediatrics medicine.medical_specialty business.industry hemic and lymphatic diseases media_common.quotation_subject medicine Haemophilia B Hematology Girl medicine.disease business media_common
Zdroj:	Thrombosis and Haemostasis. :552-557
ISSN:	2567-689X 0340-6245
DOI:	10.1055/s-0038-1655404
Popis:	SummaryA 6 year old girl with symptoms of severe haemophilia and a haemophilia B factor B content of 2%—3% of normal is described. Investigation of the family revealed that the mother and the sister of the girl were carriers of the haemophilia B gene, while the father was normal. Chromosome studies showed a pattern of 2 X chromosomes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::aaa551cec68cf84b42bc909faac809bd https://doi.org/10.1055/s-0038-1655404 Zobrazit plný text záznamu