Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier

Molecular Cytogenetics

Volumn 2, Issue 1, 2009, Pages

  Mantzouratou, Anna ^a,b   Mania, Anastasia ^a   Apergi, Marianna ^a   Laver, Sarah ^b   Serhal, Paul ^b   Delhanty, Jda ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 22; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; EMBRYO; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROZYGOTE; HUMAN; HUMAN CELL; LYMPHOCYTE; MEIOSIS; MITOSIS; MOSAICISM; OOCYTE DEVELOPMENT; PARTIAL MONOSOMY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RING CHROMOSOME;

EID: 63449111970     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-2-3     Document Type: Article

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