Familial pericentric inversion of chromosome 18: Behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome

European Journal of Human Genetics

Volumn 13, Issue 1, 2005, Pages 52-58

  Vermeulen, Stefan J ^a   Speleman, Frank ^a   Vanransbeeck, Leen ^a   Verspeet, Jasmien ^a   Menten, Björn ^a   Verschraegen Spae, Marie Rose ^a   De Wilde, Philippe ^a   Messiaen, Ludwine ^a   Michaelis, Ron C ^b   Leroy, Jules G ^a,b  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b GREENWOOD GENETIC CENTER   (United States)

Author keywords

Learning deficit; Mild phenotype; Recombinant chromosome 18; Social interaction deficit

Indexed keywords

ADOLESCENT; ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CHROMOSOME 18; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; FAMILIAL DISEASE; FEMALE; GENETIC COUNSELING; GENETIC RECOMBINATION; GENETIC RISK; HETEROZYGOTE; HUMAN; INFERTILITY; LEARNING DISORDER; MENTAL DEFICIENCY; MULTIFACTORIAL GENETIC DISORDER; PERICENTRIC CHROMOSOME INVERSION; PERSONALITY DISORDER; PHENOTYPE; PRIORITY JOURNAL; PROBABILITY; PROGENY; RECURRENCE RISK; SOCIAL INTERACTION; SOCIOPATHY; TELOMERE;

ADOLESCENT; AGED; AGED, 80 AND OVER; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; GENE DUPLICATION; HETEROZYGOTE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; KARYOTYPING; MALE; MENTAL DISORDERS; PEDIGREE; RECOMBINATION, GENETIC;

EID: 19944431941     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201281     Document Type: Article

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