Kết quả tìm kiếm - Reed, Anita AC

Proliferation Rates of Multiple Endocrine Neoplasia Type 1 (MEN1)-Associated Tumors Bằng Walls, Gerard V., Reed, Anita A.C., Jeyabalan, Jeshmi, Javid, Mahsa, Hill, Nathan R., Harding, Brian, Thakker, Rajesh V.

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Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum Bằng Williams, Siân E., Reed, Anita A.C., Galvanovskis, Juris, Antignac, Corinne, Goodship, Tim, Karet, Fiona E., Kotanko, Peter, Lhotta, Karl, Morinière, Vincent, Williams, Paul, Wong, William, Rorsman, Patrik, Thakker, Rajesh V.

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MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)) Bằng Kennedy, Ann M., Inada, Masaki, Krane, Stephen M., Christie, Paul T., Harding, Brian, López-Otín, Carlos, Sánchez, Luis M., Pannett, Anna A.J., Dearlove, Andrew, Hartley, Claire, Byrne, Michael H., Reed, Anita A.C., Nesbit, M. Andrew, Whyte, Michael P., Thakker, Rajesh V.

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Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 Bằng Nesbit, M. Andrew, Hannan, Fadil M., Howles, Sarah A., Reed, Anita A.C., Cranston, Treena, Thakker, Clare E., Gregory, Lorna, Rimmer, Andrew J., Rust, Nigel, Graham, Una, Morrison, Patrick J., Hunter, Steven J., Whyte, Michael P., McVean, Gil, Buck, David, Thakker, Rajesh V.

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Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis Bằng Gorvin, Caroline M, Loh, Nellie Y, Stechman, Michael J, Falcone, Sara, Hannan, Fadil M, Ahmad, Bushra N, Piret, Sian E, Reed, Anita AC, Jeyabalan, Jeshmi, Leo, Paul, Marshall, Mhairi, Sethi, Siddharth, Bass, Paul, Roberts, Ian, Sanderson, Jeremy, Wells, Sara, Hough, Tertius A, Bentley, Liz, Christie, Paul T, Simon, Michelle M, Mallon, Ann‐Marie, Schulz, Herbert, Cox, Roger D, Brown, Matthew A, Huebner, Norbert, Brown, Steve D, Thakker, Rajesh V

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