Homozygous PTEN deletion in neuroblastoma arising in a child with Cowden syndrome

American Journal of Medical Genetics, Part A

Volumn 155, Issue 7, 2011, Pages 1763-1766

  Bourdeaut, Franck ^a,b,c   Isidor, Bertrand ^a   Ferrand, Sandrine ^b   Thomas, Caroline ^a   Moreau, Anne ^a,d   Leclair, Marc David ^a,d   David, Albert ^a   Pierron, Gaelle ^b   Le Caignec, Cedric ^a,d,e   Delattre, Olivier ^b  

^a NANTES UNIVERSITY HOSPITAL   (France)

^b INSTITUT CURIE   (France)

^c INSTITUT CURIE   (France)

^d UNIVERSITÉ DE NANTES   (France)

^e L INSTITUT DU THORAX   (France)

Author keywords

Cowden; Neuroblastoma; Predisposition; PTEN

Indexed keywords

PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ABDOMINAL PAIN; CASE REPORT; CHILD; CHROMOSOME 10Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; COWDEN SYNDROME; DISEASE ASSOCIATION; FEMALE; GENE DELETION; HETEROZYGOTE; HISTOPATHOLOGY; HOMOZYGOTE; HUMAN; HUMAN TISSUE; LETTER; MACROCEPHALY; NEUROBLASTOMA; PRIORITY JOURNAL; RETROPERITONEAL TUMOR; THYROID TUMOR;

EID: 79959518896     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34066     Document Type: Letter

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