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Results: 1-5 |
Results: 5

Authors: Bitner-Glindzicz, M Lindley, KJ Rutland, P Blaydon, D Smith, VV Milla, PJ Hussain, K Furth-Lavi, J Cosgrove, KE Shepherd, RM Barnes, PD O'Brien, RE Farndon, PA Sowden, J Liu, XZ Scanlan, MJ Malcolm, S Dunne, MJ Aynsley-Green, A Glaser, B
Citation: M. Bitner-glindzicz et al., A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene, NAT GENET, 26(1), 2000, pp. 56-60

Authors: Dean, JC Fitzpatrick, DR Farndon, PA Kingston, H Cusine, D
Citation: Jc. Dean et al., Genetic registers in clinical practice: a survey of UK clinical geneticists, J MED GENET, 37(8), 2000, pp. 636-640

Authors: Zonana, J Elder, ME Schneider, LC Orlow, SJ Moss, C Golabi, M Shapira, SK Farndon, PA Wara, DW Emmal, SA Ferguson, BM
Citation: J. Zonana et al., A novel X-linked disorder of immune deficiency and hypohidrotic ectodermaldysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO), AM J HU GEN, 67(6), 2000, pp. 1555-1562

Authors: Cozzi, J Conn, CM Harper, J Winston, RML Rindl, M Farndon, PA Delhanty, JDA
Citation: J. Cozzi et al., A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception, HUM GENET, 104(1), 1999, pp. 23-28

Authors: Brackley, KJ Farndon, PA Weaver, JB Dow, DJ Chapman, S Kilby, MD
Citation: Kj. Brackley et al., Prenatal diagnosis of tuberous sclerosis with intracerebral signs at 14 weeks' gestation, PRENAT DIAG, 19(6), 1999, pp. 575-579
Risultati: 1-5 |