Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation

American Journal of Human Genetics

Volumn 60, Issue 1, 1997, Pages 113-120

  Wong, Andrew C C ^a   Ning, Yi ^b   Flint, Jonathan ^c   Clark, Kevin ^c   Dumanski, Jan P ^d   Ledbetter, David H ^b,e   McDermid, Heather E ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^d KAROLINSKA INSTITUTE   (Sweden)

^e UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 22Q; CONTROLLED STUDY; COSMID; GENE DELETION; GENE ISOLATION; GENE LOCUS; GENE MAPPING; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; MALE; MENTAL DEFICIENCY; MOLECULAR GENETICS; PRIORITY JOURNAL; TELOMERE; VARIABLE NUMBER OF TANDEM REPEAT;

CELL LINE, TRANSFORMED; CEREBROSIDE-SULFATASE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; CLONING, MOLECULAR; COSMIDS; ELECTROPHORESIS, GEL, PULSED-FIELD; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; SEQUENCE DELETION; TELOMERE;

EID: 0031020786     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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