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Publications
12
Citations
2.6K
H-Index
12
Active since
2010
Lorna Gregory is an author at Centre for Human Genetics specializing in medicine, genetics, and cell biology.
Publications per year
2010–2014
12
12
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3
M. Andrew Nesbit, Fadil Hannan, Sarah Howles et al. · Nature Genetics · 2012 · 279 citations · Full text
Molecular Physiology, Mendelian Disorder, Genetic Disorder +4
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
Elise Ruark, Katie Snape, Peter Humburg et al. · Nature · 2012 · 256 citations · Full text
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