Molecular Cytogenetics Protocols and Applications

Por Willatt, L.
Publicado em 2003

Cancer cytogenetics: methods and protocols

Por Willatt, L
Publicado em 2004

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

Por Willatt, L., Green, A., Trump, D.
Publicado em 2001

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

Por Dee, S., Clark, A., Willatt, L., Yates, J.
Publicado em 2001

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

Por Cornish, K, Cross, G, Green, A, Willatt, L, Bradshaw, J
Publicado em 1999

Three cases of 16q duplication.

Por Maher, E R, Willatt, L, Cuthbert, G, Chapman, C, Hodgson, S V
Publicado em 1991

Germline duplication of chromosome 2p and neuroblastoma.

Por Patel, J S, Pearson, J, Willatt, L, Andrews, T, Beach, R, Green, A
Publicado em 1997

Flecked retina associated with ring 17 chromosome.

Por Charles, S J, Moore, A T, Davison, B C, Dyson, H M, Willatt, L
Publicado em 1991

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

Por SELTMANN, M, HARRINGTON, P, PONDER, B, WILLATT, L, HEPPELL-PARTON, A, ANTON-CULVER, H
Publicado em 2000

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

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

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

Por 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
Publicado em 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

Por 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
Publicado em 2002

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

Por 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
Publicado em 1998

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

Por 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
Publicado em 2008

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

Por 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.
Publicado em 2009