Simultaneous, multilocus FISH analysis for detection of microdeletions in the diagnostic evaluation of developmental delay and mental retardation

American Journal of Human Genetics

Volumn 61, Issue 1, 1997, Pages 51-59

  Ligon, Azra H ^a   Beaudet, Arthur L ^a   Shaffer, Lisa G ^a,b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME G BAND; CONTROLLED STUDY; CYTOGENETICS; DEVELOPMENTAL DISORDER; DIGEORGE SYNDROME; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; KARYOTYPE; MAJOR CLINICAL STUDY; MENTAL RETARDATION MALFORMATION SYNDROME; MULTIPLE MALFORMATION SYNDROME; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME; WILLIAMS BEUREN SYNDROME;

EID: 0030765306     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/513904     Document Type: Article

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