TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion

American Journal of Medical Genetics, Part A

Volumn 164, Issue 3, 2014, Pages 828-833

  Palumbo, Orazio ^a   Fichera, Marco ^b   Palumbo, Pietro ^a,c   Rizzo, Renata ^d   Mazzolla, Elisabetta ^b   Cocuzza, Donatella Maria ^d   Carella, Massimo ^a   Mattina, Teresa ^b  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b UNIVERSITY OF CATANIA   (Italy)

^c UNIVERSITY OF BARI   (Italy)

^d UNIVERSITY OF CATANIA   (Italy)

Author keywords

2q24.2; Smallest region of overlap; SNP Arrays analysis; TBR1

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CLINICAL FEATURE; COMPARATIVE STUDY; FUNNEL CHEST; GENE; GROWTH RETARDATION; HUMAN; INTELLECTUAL IMPAIRMENT; INTERSTITIAL CHROMOSOME DELETION; INTERSTITIAL CHROMOSOME DELETION 2Q24; MALE; MICROARRAY ANALYSIS; MICROCEPHALY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PTOSIS; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TBR1 GENE;

2Q24.2; SMALLEST REGION OF OVERLAP; SNP ARRAYS ANALYSIS; TBR1;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 2; COMPARATIVE GENOMIC HYBRIDIZATION; GENETIC ASSOCIATION STUDIES; HUMANS; INTELLECTUAL DISABILITY; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; T-BOX DOMAIN PROTEINS;

EID: 84894235667     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.36363     Document Type: Article

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