2002•Journal of Molecular MedicineRequires access

Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p

Peter Lichtner, Tania Attié‐Bitach, Simone Schuffenhauer, Judy Henwood, Patrice Bouvagnet, Peter Scambler, Thomas Meitinger, Michel Vekemans

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Key concepts: Haploinsufficiency, Monosomy, Hypoparathyroidism, Biology, Hypoplasia, DiGeorge syndrome, Chromosomal region, Genetics

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Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p — Research Paper | ScholarLens