Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

J.M. Lapierre(Hôpital Robert-Debré), Gérard Tachdjian, Nathalie Collot(Inserm), Alain Aurias(Inserm), B. Benzaken, F. Da Silva, Serge Romana(Centre National de la Recherche Scientifique), Dennis J. Rivet(Virginia Commonwealth University), Nadège Hervy, V Cacheux, J. Wiss
PubMed
January 1, 1998
Cited by 34

Related Papers

<i>LMO2</i> -Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1
|Science|2003|3.5k
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
|Journal of Medical Genetics|1997|1.2k
Multiple Cytokines and Acute Inflammation Raise Mouse Leptin Levels: Potential Role in Inflammatory Anorexia
|The Journal of Experimental Medicine|1997|797
The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children
|Blood|2007|278
The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families
|Human Genetics|1983|189