A novel interstitial microdeletion of 7q22.1-7q22.3 detected by array comparative genomic hybridization

American Journal of Medical Genetics, Part A

Volumn 155, Issue 12, 2011, Pages 3128-3131

  Al Hassnan, Zuhair N ^a,b   Al Bakheet, Albandary ^a   Abu Dheim, Nada ^a   Al Younes, Banan ^a   Colak, Dilek ^a   Kaya, Namik ^a  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^b ALFAISAL UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

REELIN;

BODY HEIGHT; BODY WEIGHT; CASE REPORT; CHILD; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DELETION 7Q22-Q23; COMPARATIVE GENOMIC HYBRIDIZATION; CORTICAL DYSPLASIA; CRYPTORCHISM; DEVELOPMENTAL DISORDER; DNA MICROARRAY; EAR MALFORMATION; FACE MALFORMATION; GENE MUTATION; HEAD CIRCUMFERENCE; HUMAN; INFANTILE HYPOTONIA; LETTER; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; RETROGNATHIA;

ABNORMALITIES, MULTIPLE; BRAIN; CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 7; COMPARATIVE GENOMIC HYBRIDIZATION; DEVELOPMENTAL DISABILITIES; HUMANS; MAGNETIC RESONANCE IMAGING; MALE;

EID: 81955167468     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.34298     Document Type: Letter

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