Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid Syndrome) and atypical teratoid/rhabdoid tumor

American Journal of Medical Genetics, Part A

Volumn 149, Issue 5, 2009, Pages 1067-1069

  Sathyamoorthi, Shyam ^a   Morales, Jaime ^b,c   Bermudez, Jose ^b   McBride, Lori ^b   Luquette, Mark ^b   McGoey, Robin ^b,c   Oates, Nora ^d   Hales, Stephen ^d   Biegel, Jaclyn A ^e   Lacassie, Yves ^b,c  

^a TULANE UNIVERSITY   (United States)

^b LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c LOUISIANA STATE UNIVERSITY HEALTH SCIENCES CENTER   (United States)

^d CHILDREN S HOSPITAL   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; CASE REPORT; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; COMPARATIVE GENOMIC HYBRIDIZATION; DISEASE ASSOCIATION; FEMALE; FRAMESHIFT MUTATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INI1 GENE; LETTER; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE IMAGING; PHELAN MCDERMID SYNDROME; PRESCHOOL CHILD; PRIORITY JOURNAL; RHABDOID TUMOR; TERATOMA; TUMOR SUPPRESSOR GENE;

BRAIN NEOPLASMS; CHROMOSOMAL PROTEINS, NON-HISTONE; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DNA-BINDING PROTEINS; FEMALE; HUMANS; INFANT; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; RHABDOID TUMOR; SYNDROME; TERATOMA; TRANSCRIPTION FACTORS;

EID: 66849101987     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32775     Document Type: Letter

References (10)

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