An Interstitial 4q Deletion with a Mosaic Complementary Ring Chromosome in a Child with Dysmorphism, Linear Skin Pigmentation, and Hepatomegaly

por Carter, J., Brittain, H., Morrogh, D., Lench, N., Waters, J. J.
Publicado 2017

A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma

por Kinsler, VA, Drury, S, Khan, A, Waelchli, R, Rukaite, G, Barnicoat, A, Lench, N, Harper, JI, O'Shaughnessy, RFL
Publicado 2015

Prostate-specific membrane antigen: evidence for the existence of a second related human gene.

por Leek, J., Lench, N., Maraj, B., Bailey, A., Carr, I. M., Andersen, S., Cross, J., Whelan, P., MacLennan, K. A., Meredith, D. M.
Publicado 1995

A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly

por Ishida, M., Cullup, T., Boustred, C., James, C., Docker, J., English, C., Lench, N., Copp, A.J., Moore, G.E., Greene, N.D.E., Stanier, P.
Publicado 2018