Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11.
DiGeorge syndrome and velo-cardio-facial syndrome are associated with deletions within 22q11. In attempting to refine the shortest region of overlap for these syndromes we have employed fluorescence in situ hybridisation. The results obtained for some probes indicate the presence of low-copy-number...
Main Authors: | Halford, S, Lindsay, E, Nayudu, M, Carey, A, Baldini, A, Scambler, P |
---|---|
Format: | Journal article |
Language: | English |
Published: |
1993
|
Similar Items
-
Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization.
by: Lindsay, E, et al.
Published: (1993) -
Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization.
by: Desmaze, C, et al.
Published: (1993) -
Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome.
by: Roberts, C, et al.
Published: (1997) -
Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.
by: Sutherland, H, et al.
Published: (1996) -
Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
by: Odent Sylvie, et al.
Published: (2011-03-01)