Statistics
Publications
1
Citations
20
H-Index
1
Active since
1998
Affiliations
Royal Children's Hospital(Current)
M J O'Neill is an author at Royal Children's Hospital specializing in axonal pathfinding, inherited disease genetics, and human genetics.
Publications per year
1998–1998
1
1
Familial Kallmann syndrome: a novel splice acceptor mutation in the KAL gene.
M J O'Neill, Bambang Tridjaja, Matthijs J. Smith et al. · PubMed · 1998 · 20 citations
1–1 of 1