Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genes

Autor: Ardern-Jones, A., Adlard, J., Ahmed, M., Attard, G., Bailey, K., Bancroft, E., Bardsley, C., Barton, D., Bartlett, M., Barwell, J., Baxter, L., Belk, R., Berg, J., Bernhard, B., Bishop, T., Boyes, L., Bradshaw, N., Brady, A.F., Brant, S., Brewer, C., Brice, G., Bromilow, G., Brooks, C., Bruce, A., Bulman, B., Burgess, L., Campbell, J., Canham, N., Castle, B., Cetnarskyj, R., Chapman, C., Claber, O., Coates, N., Cole, T., Collins, A., Cook, J., Coulson, S., Crawford, G., Cruger, D., Cummings, C., D’Mello, L., Davidson, R., Day, L., Dell, B., Dolling, C., Donaldson, A., Dorkins, H., Douglas, F., Downing, S., Drummond, S., Dubras, C., Dunlop, J., Durrell, S., Eccles, D., Eddy, C., Edwards, M., Edwards, E., Edwardson, J., Eeles, R., Ellis, I., Elmslie, F., Evans, G., Gibbons, B., Gardiner, C., Ghali, N., Giblin, C., Gibson, S., Goff, S., Goodman, S., Goudie, D., Greenhalgh, L., Grier, J., Gregory, H., Halliday, S., Hardy, R., Hartigan, C., Heaton, T., Henderson, A., Higgins, C., Hodgson, S., Homfray, T., Horrigan, D., Houghton, C., Houlston, R.S., Hughes, L., Hunt, V., Irvine, L., Izatt, L., Jacobs, C., James, S., James, M., Jeffers, L., Jobson, I., Jones, W., Kennedy, M.J., Kenwrick, S., Kightley, C., Kirk, C., Kirk, E., Kivuva, E., Kohut, K., Kosicka-Slawinska, M., Kulkarni, A., Kumar, A., Lalloo, F., Lambord, N., Langman, C., Leonard, P., Levene, S., Locker, S., Logan, P., Longmuir, M., Lucassen, A., Lyus, V., Magee, A., Male, A., Mansour, S., McBride, D., McCann, E., McConnell, V., McEntagart, M., McKeown, C., McLeish, L., McLeod, D., Melville, A., Mercer, L., Mercer, C., Miedzybrodzka, Z., Mitra, A., Morrison, P.J., Murday, V., Murray, A., Myhill, K., Myring, J., O'Hara, E., Paterson, J., Pearson, P., Pichert, G., Platt, K., Porteous, M., Pottinger, C., Price, S., Protheroe, L., Pugh, S., Quarrell, O., Randhawa, K., Riddick, C., Robertson, L., Robinson, A., Roffey-Johnson, V., Rogers, M., Rose, S., Rowe, S., Schofield, A., Rahman, N., Saya, S., Scott, G., Scott, J., Searle, A., Shanley, S., Sharif, S., Shaw, A., Shaw, J., Shea-Simonds, J., Side, L., Sillibourne, J., Simon, K., Simpson, S., Slater, S., Smalley, S., Smith, K., Snadden, L., Snape, K., Soloway, J., Stait, Y., Stayner, B., Steel, M., Steel, C., Stewart, H., Stirling, D., Thomas, M., Thomas, S., Tomkins, S., Turner, H., Vandersteen, A., Wakeling, E., Waldrup, F., Walker, L., Watt, C., Watts, S., Webber, A., Whyte, C., Wiggins, J., Williams, E., Winchester, L., Loveday, C., Garrett, A., Law, P., Hanks, S., Poyastro-Pearson, E., Adlard, J.W., Rogers, M.T., Evans, D.G., Hanson, H., Turnbull, C.

Publikováno v: In Annals of Oncology December 2022 33(12):1318-1327

Etiology of azoospermia in 100 consecutive, non-vasectomized men

Autor: Fedder, Jens, Crüger, D., Østergaard, B., Petersen, G. Bruun

Publikováno v: Fedder, J, Crüger, D, Østergaard, B & Petersen, G B 2004, ' Etiology of azoospermia in 100 consecutive, non-vasectomized men ', Fertility and Sterility, vol. 82, pp. 1463-1465 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3062::c2888c3494db40da8aa827040101553d
https://portal.findresearcher.sdu.dk/da/publications/2283bc30-fc7a-11db-9e98-000ea68e967b

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Quantitative evaluation of fluorescence in situ hybridization (FISH) signals in uncultured coelomic cells.

Autor: Crüger, D. G., Bruun-Petersen, G., Kølvraa, S., Crüger, D G, Kølvraa, S

Publikováno v: Prenatal Diagnosis; Jul1997, Vol. 17 Issue 7, p635-642, 8p

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