AAAAAA
Results:
1-8
|
Results: 8
Authors:
Dean, JCS
Moore, SJ
Turnpenny, PD
Citation: Jcs. Dean et al., Developing diagnostic criteria for the fetal anticonvulsant syndromes, SEIZURE-E J, 9(3), 2000, pp. 233-234
Authors:
Lee, WL
Biervert, C
Hallmann, K
Tay, A
Dean, JCS
Steinlein, OK
Citation: Wl. Lee et al., A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family, NEUROPEDIAT, 31(1), 2000, pp. 9-12
Authors:
Moore, SJ
Turnpenny, P
Quinn, A
Glover, S
Lloyd, DJ
Montgomery, T
Dean, JCS
Citation: Sj. Moore et al., A clinical study of 57 children with fetal anticonvulsant syndromes, J MED GENET, 37(7), 2000, pp. 489-497
Authors:
Yong, DEJ
Booth, P
Baruni, J
Massie, D
Stephen, G
Couzin, D
Dean, JCS
Citation: Dej. Yong et al., Chromosome 22q11 microdeletion and congenital heart disease - a survey in a paediatric population, EUR J PED, 158(7), 1999, pp. 566-570
Authors:
Moore, SJ
Strain, L
Cole, GF
Miedzybrodzka, Z
Kelly, KF
Dean, JCS
Citation: Sj. Moore et al., Fragile X syndrome with FMR1 and FMR2 deletion, J MED GENET, 36(7), 1999, pp. 565-566
Authors:
Moore, SJ
Auchterlonie, IA
Cole, GF
Gray, ES
Dean, JCS
Citation: Sj. Moore et al., Partial lipodystrophy presenting with myopathy, DEVELOP MED, 41(2), 1999, pp. 127-131
Authors:
Yule, SR
Hobson, EE
Dean, JCS
Gilbert, FJ
Citation: Sr. Yule et al., Protrusio acetabuli in Marfan's syndrome, CLIN RADIOL, 54(2), 1999, pp. 95-97
Authors:
Dean, JCS
Moore, SJ
Osborne, A
Howe, J
Turnpenny, PD
Citation: Jcs. Dean et al., Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene, CLIN GENET, 56(3), 1999, pp. 216-220
Risultati:
1-8
|