Molecular Cytogenetics Protocols and Applications

द्वारा Willatt, L.
प्रकाशित 2003

Cancer cytogenetics: methods and protocols

द्वारा Willatt, L
प्रकाशित 2004

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

द्वारा Willatt, L., Green, A., Trump, D.
प्रकाशित 2001

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

द्वारा Dee, S., Clark, A., Willatt, L., Yates, J.
प्रकाशित 2001

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

द्वारा Cornish, K, Cross, G, Green, A, Willatt, L, Bradshaw, J
प्रकाशित 1999

Three cases of 16q duplication.

द्वारा Maher, E R, Willatt, L, Cuthbert, G, Chapman, C, Hodgson, S V
प्रकाशित 1991

Germline duplication of chromosome 2p and neuroblastoma.

द्वारा Patel, J S, Pearson, J, Willatt, L, Andrews, T, Beach, R, Green, A
प्रकाशित 1997

Flecked retina associated with ring 17 chromosome.

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

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

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

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

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

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

द्वारा 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
प्रकाशित 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

द्वारा 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
प्रकाशित 2002

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

द्वारा 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
प्रकाशित 1998

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

द्वारा 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
प्रकाशित 2008

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

द्वारा 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.
प्रकाशित 2009