Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22

American Journal of Medical Genetics

Volumn 86, Issue 2, 1999, Pages 168-173

  Verheij, Joke B G M ^a   Bouman, Katelÿne ^a   Van Lingen, Richard A ^b   Van Lookeren Campagne, Joannes G ^b   Leegte, Beike ^a   Van Der Veen, Anneke Y ^a   Hofstra, Robert M W ^a   Buys, Charles H C M ^a   Van Essen, Anthonie J ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b Department of Medical Genetics ^*

Author keywords

De novo origin; Intrachromosomal triplication; Partial tetrasomy 9p

Indexed keywords

ARTICLE; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASE; CHROMOSOME 9P; FACE MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; ISOCHROMOSOME; MALE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; TETRASOMY;

ADULT; ANEUPLOIDY; CENTRAL NERVOUS SYSTEM; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 9; FACE; FEMALE; FETUS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; PHENOTYPE; PREGNANCY; PSYCHOMOTOR DISORDERS;

EID: 0033543469     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990910)86:2<168::AID-AJMG16>3.0.CO;2-Q     Document Type: Article

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