Mosaic trisomy 21/monosomy 21 in a living female infant

Cytogenetic and Genome Research

Volumn 125, Issue 1, 2009, Pages 26-32

  Nguyen, H P ^a   Riess, A ^a   Kruger M ^a   Bauer, P ^a   Singer, S ^a   Schneider, M ^b   Enders, H ^a   Dufke, A ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b Genetikum   (Germany)

Author keywords

Isochromosome 21; Monosomy 21; Mosaicism

Indexed keywords

ARTICLE; AUTOSOME MOSAICISM; CASE REPORT; CHILD; CLINICAL FEATURE; DOWN SYNDROME; FACE DYSMORPHIA; FEMALE; FIBROBLAST; HUMAN; HUMAN CELL; INFANT; KARYOTYPE; LYMPHOCYTE; MONOSOMY; MONOSOMY 21; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN BIOPSY; TRISOMY 21; CHROMOSOME 21; CRANIOFACIAL MALFORMATION; GENETICS; ISOCHROMOSOME; KARYOTYPING; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PHENOTYPE; SKIN; ULTRASTRUCTURE;

MICROSATELLITE DNA;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 21; CRANIOFACIAL ABNORMALITIES; DOWN SYNDROME; FEMALE; FIBROBLASTS; HUMANS; ISOCHROMOSOMES; KARYOTYPING; LYMPHOCYTES; MICROSATELLITE REPEATS; MONOSOMY; MOSAICISM; PHENOTYPE; SKIN;

EID: 67849126897     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000218745     Document Type: Article

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