Characterisation of interstitial duplications and triplications of chromosome 15q11-q13

Human Genetics

Volumn 110, Issue 3, 2002, Pages 227-234

  Roberts, Siân E ^a,b   Dennis, Nicholas R ^b   Browne, Caroline E ^a   Willatt, Lionel ^c   Woods, C Geoffrey ^d   Cross, Ian ^e   Jacobs, Patricia A ^a,b   Thomas, N Simon ^a,b  

^a SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^b UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^c ADDENBROOKE S HOSPITAL   (United Kingdom)

^d ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

^e NEWCASTLE UPON TYNE HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; BEHAVIOR DISORDER; CHROMOSOME 15Q; CHROMOSOME 15Q11-13; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME G BAND; CHROMOSOME REARRANGEMENT; CHROMOSOME STRUCTURE; DEVELOPMENTAL DISORDER; FAMILIAL DISEASE; FEMALE; GENE LOCUS; HAPPY PUPPET SYNDROME; HUMAN; MALE; MEIOSIS; MICROSATELLITE INSTABILITY; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

ADULT; ANGELMAN SYNDROME; CHILD; CHILD BEHAVIOR DISORDERS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; DEVELOPMENTAL DISABILITIES; FEMALE; GENE DUPLICATION; GENE REARRANGEMENT; HUMANS; MALE; MEIOSIS; PEDIGREE; PHENOTYPE; PRADER-WILLI SYNDROME; RECOMBINATION, GENETIC;

EID: 0036523933     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-002-0678-6     Document Type: Article

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