A 39-bp deletion polymorphism in PTEN in African American individuals. Implications for molecular diagnostic testing

Journal of Molecular Diagnostics

Volumn 4, Issue 2, 2002, Pages 114-117

  Zhou, Xiao Ping ^a   Hampel, Heather ^a   Roggenbuck, Jennifer ^c   Saba, Nabil ^c   Prior, Thomas W ^b   Eng, Charis ^a,d  

^a OHIO STATE UNIVERSITY   (United States)

^b OHIO STATE UNIVERSITY   (United States)

^c UNIVERSITY OF MINNESOTA   (United States)

^d UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ARTICLE; ASIAN; CAUCASIAN; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; COWDEN SYNDROME; DELETION MUTANT; DIAGNOSTIC TEST; DNA FLANKING REGION; EXON; GENE DELETION; GENE LOCATION; GENETIC POLYMORPHISM; HETEROZYGOTE; HETEROZYGOTE DETECTION; HUMAN; HUMAN CELL; MUTATIONAL ANALYSIS; NEGRO; NUCLEOTIDE SEQUENCE; PROTEIN PROCESSING;

EID: 0036099838     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1525-1578(10)60690-3     Document Type: Article

References (26)

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