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Results:
1-8
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Results: 8
Authors:
Cockwell, AE
Davalos, IP
Rivera, HR
Crolla, JA
Citation: Ae. Cockwell et al., FISH characterization of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation, AM J MED G, 103(4), 2001, pp. 289-294
Authors:
Llerena, JC
de Almeida, JCC
Bastos, E
Crolla, JA
Citation: Jc. Llerena et al., FISH studies in a girl with sporadic aniridia and an apparently balanced de novo t(11;13)(p13;q33) translocation detect a microdeletion involving theWAGR region, GENET MOL B, 23(3), 2000, pp. 535-539
Authors:
Rivera, H
Correa-Cerro, LS
Robinson, DO
Crolla, JA
Citation: H. Rivera et al., Functional Xp disomy and hypomelanosis of Ito, ARCH MED R, 31(1), 2000, pp. 88-92
Authors:
Cockwell, AE
Gibbons, B
Moore, IE
Crolla, JA
Citation: Ae. Cockwell et al., An analphoid supernumerary marker chromosome derived from chromosome 3 ascertained in a fetus with multiple malformations, J MED GENET, 37(10), 2000, pp. 807-809
Authors:
Warburton, PE
Dolled, M
Mahmood, R
Alonso, A
Li, SL
Naritomi, K
Tohma, T
Nagai, T
Hasegawa, T
Ohashi, H
Govaerts, LCP
Eussen, BHJ
Van Hemel, JO
Lozzio, C
Schwartz, S
Dowhanick-Morrissette, JJ
Spinner, NB
Rivera, H
Crolla, JA
Yu, CY
Warburton, D
Citation: Pe. Warburton et al., Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere, AM J HU GEN, 66(6), 2000, pp. 1794-1806
Authors:
Thomas, NS
Browne, CE
Oley, C
Healey, S
Crolla, JA
Citation: Ns. Thomas et al., Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region, HUM GENET, 105(5), 1999, pp. 384-387
Authors:
Rivera, H
Vasquez, AI
Garcia-Cruz, D
Crolla, JA
Citation: H. Rivera et al., Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break, AM J MED G, 85(4), 1999, pp. 385-388
Authors:
Robinson, DO
Dalton, P
Jacobs, PA
Mosse, K
Power, MM
Skuse, DH
Crolla, JA
Citation: Do. Robinson et al., A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome, J MED GENET, 36(4), 1999, pp. 279-284
Risultati:
1-8
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