The human genome puzzle - the role of copy number variation in somatic mosaicism

Current Genomics

Volumn 11, Issue 6, 2010, Pages 426-431

  Mkrtchyan, Hasmik ^a,b   Gross, Madeleine ^a,i   Hinreiner, Sophie ^a,j   Polytiko, Anna ^c   Manvelyan, Marina ^a,b,d   Mrasek, Kristin ^a   Kosyakova, Nadezda ^a   Ewers, Elisabeth ^a   Nelle, Heike ^a   Liehr, Thomas ^a   Bhatt, Samarth ^a   Thoma, Karen ^e   Gebhart, Erich ^e   Wilhelm, Sylvia ^f   Fahsold, Raimund ^g   Volleth, Marianne ^h   Weise, Anja ^a  

^a JENA UNIVERSITY HOSPITAL   (Germany)

^b YEREVAN STATE UNIVERSITY   (Armenia)

^c National Medical Center Mother and Child   (Belarus)

^d Department of Medical Genetic Service ^*  (Armenia)

^e UNIVERSITY HOSPITAL ERLANGEN   (Germany)

^f Biomedical Center   (Germany)

^g Middle German Practice Group   (Germany)

^h Institute of Human Genetics   (Germany)

ⁱ GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^j Institute of Functional Genomics   (Germany)

more..

Author keywords

Copy number variations; Mosaicism; Pod FISH

Indexed keywords

ARTICLE; CELL TYPE; COPY NUMBER VARIATION; EMBRYO DEVELOPMENT; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN GENOME; INDEL MUTATION; LYMPHOBLASTOID CELL LINE; MITOSIS; MONOZYGOTIC TWINS; MOSAICISM; NONHUMAN; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 78650002534     PISSN: 13892029     EISSN: None     Source Type: Journal    
DOI: 10.2174/138920210793176047     Document Type: Article

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