Clinical profile of a male with Rett syndrome

Brain and Development

Volumn 27, Issue SUPPL. 1, 2005, Pages

  Budden, Sarojini S ^a   Dorsey, Heather C ^a   Steiner, Robert D ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

Autism; Gall bladder; Male; MECP2 mutation; Osteoporosis; Recurrent Rett syndrome

Indexed keywords

METHYL CPG BINDING PROTEIN 2;

BLADDER DISEASE; CASE REPORT; CHILD; CONFERENCE PAPER; DEVELOPMENTAL DISORDER; FAMILY HISTORY; GENDER; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HAND MOVEMENT; HETEROZYGOTE; HUMAN; MALE; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; NEUROLOGIC EXAMINATION; OSTEOPOROSIS; RETT SYNDROME; SCOLIOSIS; SEIZURE; SIBLING; SLEEP DISORDER; STEREOTYPY; VESTIBULAR DISORDER; X CHROMOSOME INACTIVATION;

CHILD; HUMANS; MALE; METHYL-CPG-BINDING PROTEIN 2; MUTATION; RETT SYNDROME; SEX CHROMOSOME ABERRATIONS;

EID: 27144478270     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.braindev.2005.03.018     Document Type: Conference Paper

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