Molecular Cytogenetics Protocols and Applications

gan Willatt, L.
Cyhoeddwyd 2003

Cancer cytogenetics: methods and protocols

gan Willatt, L
Cyhoeddwyd 2004

Satellites on the terminal short arm of chromosome 12 (12ps), inherited through several generations in three families: a new variant without phenotypic effect

gan Willatt, L., Green, A., Trump, D.
Cyhoeddwyd 2001

A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH

gan Dee, S., Clark, A., Willatt, L., Yates, J.
Cyhoeddwyd 2001

A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis

gan Cornish, K, Cross, G, Green, A, Willatt, L, Bradshaw, J
Cyhoeddwyd 1999

Three cases of 16q duplication.

gan Maher, E R, Willatt, L, Cuthbert, G, Chapman, C, Hodgson, S V
Cyhoeddwyd 1991

Germline duplication of chromosome 2p and neuroblastoma.

gan Patel, J S, Pearson, J, Willatt, L, Andrews, T, Beach, R, Green, A
Cyhoeddwyd 1997

Flecked retina associated with ring 17 chromosome.

gan Charles, S J, Moore, A T, Davison, B C, Dyson, H M, Willatt, L
Cyhoeddwyd 1991

A case of inv dup(8p) with early onset breast cancer

gan SELTMANN, M, HARRINGTON, P, PONDER, B, WILLATT, L, HEPPELL-PARTON, A, ANTON-CULVER, H
Cyhoeddwyd 2000

A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line.

gan Willatt, L R, Davison, B C, Goudie, D, Alexander, J, Dyson, H M, Jenks, P E, Ferguson-Smith, M E
Cyhoeddwyd 1992

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation...

gan Shaw-Smith, C, Redon, R, Rickman, L, Rio, M, Willatt, L, Fiegler, H, Firth, H, Sanlaville, D, Winter, R, Colleaux, L, Bobrow, M, Carter, N
Cyhoeddwyd 2004

A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation

gan Borg, I, Squire, M, Menzel, C, Stout, K, Morgan, D, Willatt, L, O'Brien, P, Ferguson-Smith, M, Ropers, H, Tommerup, N, Kalscheuer, V, Sargan, D
Cyhoeddwyd 2002

Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

gan Barber, J C, Joyce, C A, Collinson, M N, Nicholson, J C, Willatt, L R, Dyson, H M, Bateman, M S, Green, A J, Yates, J R, Dennis, N R
Cyhoeddwyd 1998

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

gan Koolen, D A, Sharp, A J, Hurst, J A, Firth, H V, Knight, S J L, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L E L M, Destrée, A, Grisart, B, Rooms, L, Aa, N Van der, Field, M, Hackett, A, Bell, K, Nowaczyk, M J M, Mancini, G M S, Poddighe, P J, Schwartz, C E, Rossi, E, De Gregori, M, Antonacci-Fulton, L L, McLellan, M D, Garrett, J M, Wiechert, M A, Miner, T L, Crosby, S, Ciccone, R, Willatt, L, Rauch, A, Zenker, M, Aradhya, S, Manning, M A, Strom, T M, Wagenstaller, J, Krepischi-Santos, A C, Vianna-Morgante, A M, Rosenberg, C, Price, S M, Stewart, H, Shaw-Smith, C, Brunner, H G, Wilkie, A O M, Veltman, J A, Zuffardi, O, Eichler, E E, de Vries, B B A
Cyhoeddwyd 2008

Further delineation of the 15q13 microdeletion and duplication syndromes: A clinical spectrum varying from non-pathogenic to a severe outcome

gan van Bon, B.W.M., Mefford, H.C., Menten, B., Koolen, D. A., Sharp, A. J., Nillesen, W.M., Innis, J.W., de Ravel, T.J.L., Mercer, C.L., Fichera, M., Stewart, H., Connell, L. E., Õunap, K., Lachlan, K., Castle, B., Van der Aa, N., van Ravenswaaij, C., Nobrega, M.A., Serra-Juhé, C, Simonic, I., de Leeuw, N., Pfundt, R., Bongers, E.M., Baker, C., Finnemore, P., Huang, S., Maloney, V.K., Crolla, J.A., van Kalmthout, M., Elia, M., Vandeweyer, G., Fryns, J.P., Janssens, S., Foulds, N., Reitano, S., Smith, K., Parkel, S., Loeys, B., Woods, C.G., Oostra, A., Speleman, F., Pereira, A.C., Kurg, A., Willatt, L., Knight, S.J.L., Vermeesch, J.R., Romano, C., Barber, J.C., Mortier, G., Pérez-Jurado, L.A., Kooy, F., Brunner, H.G., Eichler, E.E., Kleefstra, T., de Vries, B.B.A.
Cyhoeddwyd 2009