Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype

Proceedings of the National Academy of Sciences of the United States of America

Volumn 100, Issue 8, 2003, Pages 4684-4689

  State, Matthew W ^a,b   Greally, John M ^d   Cuker, Adam ^c   Bowers, Peter N ^b   Henegariu, Octavian ^b   Morgan, Thomas M ^b   Gunel, Murat ^b   DiLuna, Michael ^b   King, Robert A ^a   Nelson, Carol ^b   Donovan, Abigail ^c   Anderson, George M ^a   Leckman, James F ^a   Hawkins, Trevor ^f   Pauls, David L ^e   Liftont, Richard P ^b   Ward, David C ^b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Department of Genetics ^*  (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^e MASSACHUSETTS GENERAL HOSPITAL   (United States)

^f U S DEPARTMENT OF ENERGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 18Q; CHROMOSOME ABERRATION; CHROMOSOME INVERSION; GENE CONTROL; GENE IDENTIFICATION; GENE MAPPING; GENE REARRANGEMENT; GENE REPLICATION; GILLES DE LA TOURETTE SYNDROME; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; TELOMERE;

CHILD; CHROMOSOME BREAKAGE; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CHROMOSOMES, HUMAN, PAIR 18; DNA REPLICATION; DNA, COMPLEMENTARY; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; MALE; MOLECULAR SEQUENCE DATA; OBSESSIVE-COMPULSIVE DISORDER; PHENOTYPE; TICS; TOURETTE SYNDROME;

EID: 0344490333     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0730775100     Document Type: Article

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