William G Newman (Glenda M Beaman)

Years Active: 2019-2021
Publications (10 Years): 3

This page only lists publications with an associated author ORCID identifier.

Publications

Nicola Flaum, Elke Maria van Veen, Olivia Smith, Stephanie Amico, William G Newman, Emma J Crosbie, Richard Edmondson, Miriam Jane Smith, D Gareth Evans
Dominant-negative pathogenic variant BRIP1 c.1045G>C is a high-risk allele for non-mucinous epithelial ovarian cancer: A case-control study. Clinical genetics 101 (1) (2021)
William G Newman, Adrian S Woolf, Raimondo M Cervellione, David Keene, Imran Mushtaq, Jill E Urquhart, Helen M Stuart, William G Newman
22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complex. American journal of medical genetics. Part A 179 (3) (2019)
William G Newman, Gabriella Galatà, Keng W Teik, Jill E Urquhart, Ali Aishah, James O'Sullivan, Sanjeev S Bhaskar, Katherine A Wood, Huw B Thomas, Raymond T O'Keefe, Adrian S Woolf, Helen M Stuart, William G Newman
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical genetics 96 (6) (2019)

William G Newman.css-eqlu8i{font-size:small;padding-left:4px;} (Glenda M Beaman)