Interstitial 3p25.3-p26.1 deletion in a patient with intellectual disability

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 10, 2012, Pages 2587-2590

  Riess, Angelika ^a   Grasshoff, Ute ^a   Schäferhoff, Karin ^a   Bonin, Michael ^a   Riess, Olaf ^a   Horber, Veronka ^b   Tzschach, Andreas ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

Author keywords

Del3p25.3 p26.1; Intellectual disability; SNP array; SRGAP3 MEGAP

Indexed keywords

DNA;

ARTICLE; CASE REPORT; CAV3 GENE; CHILD; CHROMOSOME 3P; CONGENITAL HEART MALFORMATION; COPY NUMBER VARIATION; DNA DETERMINATION; EPILEPSY; FACE MALFORMATION; FEMALE; GENE; GENE LOCATION; GENETIC ASSOCIATION; GENOME SIZE; GENOTYPE PHENOTYPE CORRELATION; HAPLOINSUFFICIENCY; HUMAN; HUMAN CELL; INTELLECTUAL IMPAIRMENT; INTERSTITIAL CHROMOSOME DELETION; LEUKOCYTE; MEGAP GENE; MICROARRAY ANALYSIS; MUSCLE HYPOTONIA; MUTATIONAL ANALYSIS; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; SINGLE NUCLEOTIDE POLYMORPHISM; SRGAP3 GENE; STRABISMUS;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 3; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENETIC ASSOCIATION STUDIES; GTPASE-ACTIVATING PROTEINS; HUMANS; INTELLECTUAL DISABILITY; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84866500694     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35562     Document Type: Article

References (8)

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