TY  - GEN
AU  - Thompson,L J
AU  - Lalloz,M R
AU  - Layton,D M
TI  - Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
SN  - 1079-9796
PY  - 1999///1229
KW  - Asian People
KW  - genetics
KW  - Black People
KW  - Family Health
KW  - Female
KW  - Genetic Carrier Screening
KW  - Haplotypes
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Polymorphism, Single-Stranded Conformational
KW  - Pregnancy
KW  - Prenatal Diagnosis
KW  - Sequence Analysis, DNA
KW  - Thrombocytopenia
KW  - United Kingdom
KW  - epidemiology
KW  - White People
KW  - Wiskott-Aldrich Syndrome
KW  - X Chromosome
N1  - Publication Type: Comparative Study; Journal Article
UR  - https://doi.org/10.1006/bcmd.1999.0247
ER  -