Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases

European Journal of Medical Genetics

Volumn 52, Issue 5, 2009, Pages 291-296

  Schluth Bolard, Caroline ^a,b   Delobel, Bruno ^c   Sanlaville, Damien ^a,b   Boute, Odile ^d   Cuisset, Jean Marie ^d   Sukno, Sylvie ^c   Labalme, Audrey ^a   Duban Bedu, Bénédicte ^c   Plessis, Ghislaine ^e   Jaillard, Sylvie ^f,g   Dubourg, Christèle ^f,g   Henry, Catherine ^f   Lucas, Josette ^f   Odent, Sylvie ^g,h   Pasquier, Laurent ^g,h   Copin, Henri ⁱ   Latour, Philippe ^a   Cordier, Marie Pierre ^a   Nadeau, Gwenaël ^j   Till, Marianne ^a   Edery, Patrick ^a,b   Andrieux, Joris ^d   more..

^a HOSPICES CIVILS DE LYON   (France)

^b UNIVERSITÉ LYON 1   (France)

^c HÔPITAL SAINT VINCENT DE PAUL   (France)

^d LILLE UNIVERSITY HOSPITAL   (France)

^e CHU Clemenceau   (France)

^f PONTCHAILLOU UNIVERSITY HOSPITAL   (France)

^g UNIVERSITÉ DE RENNES 1   (France)

^h SERVICE DE RHUMATOLOGIE   (France)

ⁱ AMIENS UNIVERSITY HOSPITAL   (France)

^j CENTRE HOSPITALIER DE VALENCE   (France)

more..

Author keywords

Abnormal phenotype; Apparently balanced translocations; Array CGH

Indexed keywords

ARTICLE; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; CONTROLLED STUDY; DNA MICROARRAY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOMICS; HUMAN; KARYOTYPE; MALE; MENTAL DEFICIENCY; PHENOTYPIC VARIATION; POLYMERASE CHAIN REACTION;

EID: 69049109727     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.05.011     Document Type: Article

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