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Results:
1-8
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Results: 8
Developing diagnostic criteria for the fetal anticonvulsant syndromes
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
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family
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
A clinical study of 57 children with fetal anticonvulsant syndromes
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
Chromosome 22q11 microdeletion and congenital heart disease - a survey in a paediatric population
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
Fragile X syndrome with FMR1 and FMR2 deletion
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
Partial lipodystrophy presenting with myopathy
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
Protrusio acetabuli in Marfan's syndrome
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
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene
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
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