The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome [4]

Journal of Medical Genetics

Volumn 38, Issue 1, 2001, Pages 52-58

  Parisi, M A ^a   Dinulos, M B ^a   Leppig, K A ^a   Sybert, V P ^a   Eng, C ^a   Hudgins, L ^a  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME PROTEIN; PHOSPHATASE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

AUTOSOMAL DOMINANT DISORDER; BANNAYAN RILEY RUVALCABA SYNDROME; CLINICAL ARTICLE; CLINICAL FEATURE; COWDEN SYNDROME; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; LETTER; MALE; NEWBORN; PHENOTYPE; PRIORITY JOURNAL; SYNDROME DELINEATION;

EID: 0035138678     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.38.1.52     Document Type: Letter

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