Prenatal diagnosis of severe factor VII deficiency using mutation detection and linkage analysis
Br J Haematol
.
2001 Jan;112(1):251-2.
doi: 10.1046/j.1365-2141.2001.02497-4.x.
Authors
M Giansily-Blaizot
,
P Aguilar-Martinez
,
C Mazurier
,
F Cneude
,
J Goudemand
,
J F Schved
,
B de Martinville
PMID:
11225604
DOI:
10.1046/j.1365-2141.2001.02497-4.x
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child, Preschool
Chromosome Mapping
DNA Mutational Analysis
Female
Fetal Diseases / diagnosis*
Hemophilia A / diagnosis*
Humans
Infant, Newborn
Pregnancy
Prenatal Diagnosis / methods*