11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity

American Journal of Medical Genetics, Part A

Volumn 155, Issue 6, 2011, Pages 1272-1280

  Shinawi, Marwan ^a,d   Sahoo, Trilochan ^a,f   Maranda, Bruno ^b   Skinner, S A ^c   Skinner, Cindy ^c   Chinault, Craig ^a   Zascavage, Roxanne ^a   Peters, Sarika U ^a,e   Patel, Ankita ^a   Stevenson, Roger E ^c   Beaudet, Arthur L ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITÉ DE SHERBROOKE   (Canada)

^c GREENWOOD GENETIC CENTER   (United States)

^d WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e PerkinElmer   (United States)

^f VANDERBILT UNIVERSITY   (United States)

Author keywords

11p14.1; ADHD; Autism; BDNF; Developmental delay; Microdeletion; Obesity; WAGR

Indexed keywords

METHYLPHENIDATE;

11P14.1 MICRODELETION; ANIRIDIA; ARM FRACTURE; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; BDNF GENE; BRACHYDACTYLY; CASE REPORT; CHILD; COGNITIVE DEFECT; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL GLAUCOMA; DEVELOPMENTAL DISORDER; EAR INFECTION; FACE DYSMORPHIA; FAILURE TO THRIVE; FAMILY HISTORY; FEEDING DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GASTROESOPHAGEAL REFLUX; GENE; GENOME ANALYSIS; HERNIA; HUMAN; INFANT; INTERSTITIAL CHROMOSOME DELETION; LEG FRACTURE; LIN7C GENE; MALE; MICROARRAY ANALYSIS; MUSCLE HYPOTONIA; NEWBORN; NYSTAGMUS; OBESITY; OSTEOPENIA; PRESCHOOL CHILD; PRIORITY JOURNAL; RECURRENT INFECTION; SINUS TACHYCARDIA; SPEECH DISORDER; URETHRA DIVERTICULUM; VITAMIN D DEFICIENCY;

ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; AUTISTIC DISORDER; CHILD; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 11; DEVELOPMENTAL DISABILITIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MICROARRAY ANALYSIS; OBESITY; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE;

EID: 79956223036     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33878     Document Type: Article

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