Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: Clinical, cytogenetic and molecular analysis

European Journal of Human Genetics

Volumn 10, Issue 11, 2002, Pages 694-698

  Velissariou, Voula ^a   Antoniadi, Thalia ^a   Gyftodimou, Jolanda ^b   Bakou, Katerina ^a   Grigoriadou, Maria ^b   Christopoulou, Stavroula ^a   Hatzipouliou, Athina ^a   Donoghue, Jackie ^a   Karatzis, Panagiotis ^a   Katsarou, Efstathia ^c   Petersen, Michael B ^b  

^a Gastroenterology Department   (Greece)

^b Institute of Child Health   (Greece)

^c P AND A KYRIAKOU CHILDREN S HOSPITAL   (Greece)

Author keywords

Imprinting; Nondisjunction; Prenatal diagnosis; Trisomy 20 mosaicism; Uniparental disomy

Indexed keywords

ADULT; AMNION FLUID; ARTICLE; BLOOD CELL; CASE REPORT; CHROMOSOME 20; CHROMOSOME MOSAICISM; CLINICAL FEATURE; CONTROLLED STUDY; CYTOGENETICS; DIPLOIDY; FEMALE; FETUS; FOLLOW UP; GROWTH RETARDATION; HUMAN; INTRAUTERINE GROWTH RETARDATION; KYPHOSIS; MOLECULAR GENETICS; MUSCLE HYPERTONIA; MUSCLE HYPOTONIA; NEWBORN; OUTCOMES RESEARCH; PHENOTYPE; PLACENTA; POSTNATAL GROWTH; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; TRISOMY 21; UNIPARENTAL DISOMY; URINE SEDIMENT; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC MARKER; GENETICS; INFANT; MOSAICISM; PSYCHOMOTOR DISORDER; TRISOMY;

CHROMOSOMES, HUMAN, PAIR 20; FEMALE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MOSAICISM; PSYCHOMOTOR DISORDERS; TRISOMY; UNIPARENTAL DISOMY;

EID: 18744405678     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200867     Document Type: Article

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