The good SHP2 association: A porthole into the genetics of congenital heart disease

Circulation: Cardiovascular Genetics

Volumn 5, Issue 3, 2012, Pages 271-273

  Gelb, Bruce D ^a   Seidman, Christine E ^b  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); PROTEIN TYROSINE PHOSPHATASE SHP 2;

ATTRIBUTABLE RISK; CHROMOSOME 12; CONGENITAL HEART DISEASE; COPY NUMBER VARIATION; FALLOT TETRALOGY; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM;

HUMANS; PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 11; TETRALOGY OF FALLOT;

EID: 84864578044     PISSN: 1942325X     EISSN: 19423268     Source Type: Journal    
DOI: 10.1161/CIRCGENETICS.112.963215     Document Type: Review

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