Isochromosome 18p results from maternal meiosis II nondisjunction

European Journal of Human Genetics

Volumn 4, Issue 3, 1996, Pages 168-174

  Kotzot, Dieter ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

Chromosome aberration, origin of; Fluorescence in situ hybridization; Isochromosome 18p; Meiotic nondisjunction; Tetrasomy 18p

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CHROMOSOME 18P; CHROMOSOME BANDING PATTERN; CLINICAL ARTICLE; FEMALE; GENE DOSAGE; HUMAN; HUMAN CELL; INHERITANCE; ISOCHROMOSOME; MALE; MARKER CHROMOSOME; MEIOSIS; MOTHER; NONDISJUNCTION; PRIORITY JOURNAL; TETRASOMY; TRISOMY 18;

ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; GENOMIC IMPRINTING; HUMANS; MALE; MEIOSIS; MICROSATELLITE REPEATS; NONDISJUNCTION, GENETIC; PEDIGREE;

EID: 0030015733     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472191     Document Type: Article

References (2)

1. Schinzel A: Human Cytogenetic Database. Oxford Medical Databases Series. Oxford, Oxford University Press, Electronic Publishing, 1994.
2. Froland A, Holst G, Terslev E: Multiple anomalies associated with an extra small autosome. Cytogenetics 1963;2:99-106.