Trisomy 21 mosaicism: We may all have a touch of down syndrome

Cytogenetic and Genome Research

Volumn 139, Issue 3, 2013, Pages 189-192

  Hulten M A ^a,c   Jonasson, J ^e   Iwarsson, E ^c,d   Uppal, P ^b,c   Vorsanova, S G ^f,g,h   Yurov, Y B ^f,g,h   Iourov, I Y ^f,g  

^a UNIVERSITY OF WARWICK   (United Kingdom)

^b IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

^c KAROLINSKA INSTITUTE   (Sweden)

^d KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^e LINKÖPING UNIVERSITY   (Sweden)

^f PIROGOV RUSSIAN NATIONAL RESEARCH MEDICAL UNIVERSITY   (Russian Federation)

^g INSTITUTE OF BIOMEDICAL CHEMISTRY   (Russian Federation)

^h MOSCOW STATE UNIVERSITY OF PSYCHOLOGY AND EDUCATION   (Russian Federation)

Author keywords

Chromosome aberration; Down syndrome; Fetus; Gonad; Mosaicism; Trisomy 21

Indexed keywords

DNA;

ALZHEIMER DISEASE; COPY NUMBER VARIATION; DISOMY; DOWN SYNDROME; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; FLUORESCENCE MICROSCOPY; HUMAN; HUMAN GENOME; LEARNING DISORDER; LYMPHOCYTE CULTURE; MOSAICISM; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; REVIEW; SUPERNUMERARY CHROMOSOME; TRISOMY 21; ZYGOTE; ARTICLE; CHROMOSOME; DISEASE PREDISPOSITION; STRUCTURAL CHROMOSOME ABERRATION;

CHROMOSOMES, HUMAN, PAIR 21; DNA COPY NUMBER VARIATIONS; DOWN SYNDROME; GENETICS, POPULATION; HUMANS; MOSAICISM;

EID: 84877578116     PISSN: 14248581     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000346028     Document Type: Review

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