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Results: 1-4 |
Results: 4

Authors: Leonard, NJ Tomkins, DJ Demianczuk, N
Citation: Nj. Leonard et al., Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat, PRENAT DIAG, 20(12), 2000, pp. 947-949

Authors: Nowaczyk, MJM Huggins, MJ Tomkins, DJ Rossi, E Ramsay, JA Woulfe, J Scherer, SW Belloni, E
Citation: Mjm. Nowaczyk et al., Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency, CLIN GENET, 57(5), 2000, pp. 388-393

Authors: Winsor, EJT Tomkins, DJ Kalousek, D Farrell, S Wyatt, P Fan, YS Carter, R Wang, HS Dallaire, L Eydoux, P Welch, JP Dawson, A Lin, JCC Singer, J Johnson, J Wilson, RD
Citation: Ejt. Winsor et al., Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluidtrial (CEMAT), PRENAT DIAG, 19(7), 1999, pp. 620-627

Authors: Sathya, P Tomkins, DJ Freeman, V Paes, B Nowaczyk, JM
Citation: P. Sathya et al., De novo deletion 12q: Report of a patient with 12q24.31q24.33 deletion, AM J MED G, 84(2), 1999, pp. 116-119
Risultati: 1-4 |