Neuropathology of 22q11 deletion syndrome in an infant

Pediatric and Developmental Pathology

Volumn 17, Issue 5, 2014, Pages 386-392

  Wu, Peter ^a   Teot, Lisa ^b   Murdoch, Geoffrey ^c   Monaghan Nichols, A Paula ^c   McFadden, Kathryn ^c  

^a UNIVERSITY OF PITTSBURGH   (United States)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

22q11 deletion syndrome; Cortex; Interstitial neurons; Neuropathology; Subplate; Velocardiofacial syndrome

Indexed keywords

BRAIN PROTEIN; NEURON SPECIFIC NUCLEAR PROTEIN; PHOSPHOPROTEIN DARPP 32; PROTEIN CTIP2; PROTEIN CUX1; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CHROMOSOME DELETION 22Q11; CONTROLLED STUDY; FALLOT TETRALOGY; FLUORESCENCE IN SITU HYBRIDIZATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; MALE; NERVE CELL; NEUROPATHOLOGY; OCCIPITAL LOBE; PULMONARY VALVE ATRESIA; WHITE MATTER; 22Q11 DELETION SYNDROME; AUTOPSY; BRAIN; CHROMOSOME 22; GENETIC PREDISPOSITION; GENETICS; PATHOLOGY; PROCEDURES;

22Q11 DELETION SYNDROME; AUTOPSY; BRAIN; CHROMOSOMES, HUMAN, PAIR 22; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; MALE; NEURONS;

EID: 84916886560     PISSN: 10935266     EISSN: 16155742     Source Type: Journal    
DOI: 10.2350/13-11-1399-CR.1     Document Type: Article

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