Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia. [electronic resource]
Producer: 19991229Description: 218-26 p. digitalISSN:- 1079-9796
- Asian People -- genetics
- Black People -- genetics
- Family Health
- Female
- Genetic Carrier Screening
- Haplotypes
- Humans
- Male
- Mutation -- genetics
- Pedigree
- Polymorphism, Single-Stranded Conformational
- Pregnancy
- Prenatal Diagnosis
- Sequence Analysis, DNA
- Thrombocytopenia -- genetics
- United Kingdom -- epidemiology
- White People -- genetics
- Wiskott-Aldrich Syndrome -- genetics
- X Chromosome
No physical items for this record
Publication Type: Comparative Study; Journal Article
There are no comments on this title.
Log in to your account to post a comment.