De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosis
Year: 1986
Type: article
Source: Human Genetics
DOI: 10.1007/bf00282556
Institutions: Hôpital Cochin, Laboratoire de Biochimie
Language: English
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2007635168
