An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12. [electronic resource]
- Haematologica Oct 2011
- 1567-8 p. digital
Publication Type: Case Reports; Letter
1592-8721
10.3324/haematol.2010.036897 doi
Alleles Base Sequence Child, Preschool Chromosomes, Human, Pair 12 Female Genotype Hematologic Tests Humans Pedigree Sequence Deletion Uniparental Disomy von Willebrand Disease, Type 3--diagnosis