Citations for
1DEL14Q32
A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: Further delineation of a critical region for the 14q32 deletion syndrome.
Holder JL Jr, Lotze TE, Bacino C, Cheung SW.
Am J Med Genet A 158A(8):1962-6. doi: 10.1002/ajmg.a.35289. Epub 2012 Apr 9. 2012
2DEL14Q32, UPD14M
A recurrent 14q32.2 microdeletion mediated by expanded TGG repeats.
Béna F, Gimelli S, Migliavacca E, Brun-Druc N, Buiting K, Antonarakis SE, Sharp AJ.
Hum Mol Genet um Mol Genet. 2010 Mar 2. [Epub ahead of print]PMID: 20179077 2010