Smith-Magenis syndrome: Clinical evaluation in seven Brazilian patients

Genetics and Molecular Research

Volumn 10, Issue 4, 2011, Pages 2664-2670

  Gamba, B F ^a   Vieira, G H ^a   Souza, D H ^a   Monteiro, F F ^a   Lorenzini, J J ^a   Carvalho, D R ^a   Morreti Ferreira, D ^a  

^a SÃO PAULO STATE UNIVERSITY UNESP   (Brazil)

Author keywords

17p11.2; Deletion; FISH; Smith Magenis syndrome

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; BRAZILIAN; CHROMOSOME 17P; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; CRANIOFACIAL MALFORMATION; EAR INFECTION; FLUORESCENCE IN SITU HYBRIDIZATION; HEARING IMPAIRMENT; HOARSENESS; HUMAN; INTELLECTUAL IMPAIRMENT; MENTAL DEFICIENCY; SMITH MAGENIS SYNDROME; STEREOTYPY; STRABISMUS; TOOTH MALFORMATION; ADOLESCENT; BRAZIL; CHILD; CHROMOSOME 17; CLINICAL TRIAL; FEMALE; GENETICS; MALE; META ANALYSIS; METHODOLOGY; PATHOLOGY; POINT MUTATION;

RAI1 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ADOLESCENT; BRAZIL; CHILD; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; MALE; POINT MUTATION; SMITH-MAGENIS SYNDROME; TRANSCRIPTION FACTORS;

EID: 84856495020     PISSN: None     EISSN: 16765680     Source Type: Journal    
DOI: 10.4238/2011.October.31.17     Document Type: Article

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