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Genetic screening / counselling
Contributing journals to this collection:
Archives of Disease in Childhood - Education and Practice,
Archives of Disease in Childhood - Fetal and Neonatal Edition,
and Archives of Disease in Childhood
Citations 11-20 of 40 total displayed.
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Perinatal lessons from the past
Gregor Mendel, OSA (18221884), founder of scientific genetics
- P M Dunn
Arch. Dis. Child. Fetal Neonatal Ed. 2003; 88: F537-F539.
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Acute paediatrics
Clinical improvement in cystic fibrosis with early insulin treatment
- L Dobson, A T Hattersley, S Tiley, S Elworthy, P J Oades, and C D Sheldon
Arch. Dis. Child. 2002; 87: 430-431.
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Leading articles
The Human Genome Project: the next decade
- R M Gardiner
Arch. Dis. Child. 2002; 86: 389-391.
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Acute paediatrics
No association between asthma or allergy and the CCR5 32 mutation
- A Nagy, G T Kozma, Á Bojszkó, D Krikovszky, A Falus, and C Szalai
Arch. Dis. Child. 2002; 86: 426.
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Community child health, public health, and epidemiology
Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study
- G R Serjeant, A Singhal, and I R Hambleton
Arch. Dis. Child. 2001; 85: 375-378.
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General and acute paediatrics
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose
- C J Hendriksz, P McClean, M J Henderson, D G Keir, V C Worthington, F Imtiaz, E Schollen, G Matthijs, and B G Winchester
Arch. Dis. Child. 2001; 85: 339-340.
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Original articles
Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies
- K Carpenter, V Wiley, K G Sim, D Heath, and B Wilcken
Arch. Dis. Child. Fetal Neonatal Ed. 2001; 85: F105-F109.
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Leading articles
Alpha-1 antitrypsin deficiency
- R A PRIMHAK and M S TANNER
Arch. Dis. Child. 2001; 85: 2-5.
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General and specialist paediatrics
Significance of fever in Jamaican patients with homozygous sickle cell disease
- K J J Wierenga, I R Hambleton, R M Wilson, H Alexander, B E Serjeant, and G R Serjeant
Arch. Dis. Child. 2001; 84: 156-159.
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Original articles
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency
- E H Touma, M S Rashed, C Vianey-Saban, A Sakr, P Divry, N Gregersen, and B S Andresen
Arch. Dis. Child. 2001; 84: 58-60.
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Genetic screening / counselling
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