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Gorvin, Caroline M, Stokes, Victoria J, Boon, Hannah, Cranston, Treena, Gluck, Anna K, Bahl, Shailini, Homfray, Tessa, Aung, Theingi, Shine, Brian, Lines, Kate E
et al (show 2 more authors) (2020) Activating Mutations of the G-protein Subunit a 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 105 (3). pp. 952-963.


Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H, Nowak, Catherine B, Douglas, Jessica, Swoboda, Kathryn J
et al (show 368 more authors) (2019) CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018). NATURE COMMUNICATIONS, 10 (1). 883-.


Bancroft, Elizabeth K, Saya, Sibel, Page, Elizabeth C, Myhill, Kathryn, Thomas, Sarah, Pope, Jennifer, Chamberlain, Anthony, Hart, Rachel, Glover, Wayne, Cook, Jackie
et al (show 327 more authors) (2019) Psychosocial impact of undergoing prostate cancer screening for men with <i>BRCA1 or BRCA2</i> mutations. BJU INTERNATIONAL, 123 (2). pp. 284-292.

This list was generated on Mon Feb 12 10:33:42 2024 GMT.