An 18-year follow-up report on an infant with a duplication of 9q34

American Journal of Medical Genetics, Part A

Volumn 152, Issue 1, 2010, Pages 230-233

  Youngs, Erin L ^a   McCord, Timothy ^a   Hellings, Jessica A ^a   Spinner, Nancy B ^b   Schneider, Adele ^c   Butler, Merlin G ^a  

^a UNIVERSITY OF KANSAS MEDICAL CENTER   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c ALBERT EINSTEIN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; DYNAMIN I; PSYCHOTROPIC AGENT; ABC TRANSPORTER; CARNITINE ACETYLTRANSFERASE; MANNOSYLTRANSFERASE; MITOGEN ACTIVATED PROTEIN KINASE 1; NOTCH1 RECEPTOR; NUCLEAR RECEPTOR NR6A1; THYROID TRANSCRIPTION FACTOR 1;

ADULT; ANTHROPOMETRY; APNEA; ARACHNODACTYLY; ARNOLD CHIARI MALFORMATION; ARTERY MALFORMATION; ATTENTION DEFICIT DISORDER; AUTISM; BEHAVIOR DISORDER; BRADYCARDIA; CAMPTODACTYLY; CELL FATE; CHROMOSOME 12; CHROMOSOME 9Q; CHROMOSOME BAND; CHROMOSOME DUPLICATION; CHROMOSOME PAINTING; DENTAL SURGERY; DNA MICROARRAY; EAR MALFORMATION; ECHOCARDIOGRAPHY; ENDOPLASMIC RETICULUM; ESTERIFICATION; FACE ASYMMETRY; FEEDING DISORDER; FOLLOW UP; FOOT MALFORMATION; FRONTAL BOSSING; GAIT DISORDER; GENE DUPLICATION; GENETIC COUNSELING; GENOTYPE PHENOTYPE CORRELATION; GROWTH RETARDATION; HAND MALFORMATION; HEART MURMUR; HUMAN; HYPERACTIVITY; HYPERREFLEXIA; IMMOBILIZATION; INTELLIGENCE QUOTIENT; KARYOTYPE 46,XY; LETTER; MALE; MICROGNATHIA; MICROPENIS; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; ORCHIDOPEXY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; SCROTUM DISORDER; SPEECH DISORDER; STRABISMUS; SUBCLAVIAN ARTERY; SUPERNUMERARY CHROMOSOME; SYNDACTYLY; TOE MALFORMATION; ANAMNESIS; BEHAVIOR CHANGE; CASE REPORT; CHILD; CHROMOSOME 9; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; DEVELOPMENTAL DISORDER; DISEASE COURSE; EYE SURGERY; GENE DELETION; GENE FUNCTION; GENOTYPE; INFANT; PRESCHOOL CHILD; PROTEIN FUNCTION; RANGE OF MOTION; SCHOOL CHILD; SUPERIOR CAVA VEIN OBSTRUCTION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 9; FOLLOW-UP STUDIES; HUMANS; INFANT; MALE;

EID: 75149121487     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33196     Document Type: Letter

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