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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.

Past content
Arch. Dis. Child. Fetal Neonatal Ed.
Perinatal lessons from the past
Gregor Mendel, OSA (1822–1884), founder of scientific genetics
P M Dunn
Arch. Dis. Child. Fetal Neonatal Ed. 2003; 88: F537-F539. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
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. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Leading articles
The Human Genome Project: the next decade
R M Gardiner
Arch. Dis. Child. 2002; 86: 389-391. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Acute paediatrics
No association between asthma or allergy and the CCR5{Delta} 32 mutation
A Nagy, G T Kozma, Á Bojszkó, D Krikovszky, A Falus, and C Szalai
Arch. Dis. Child. 2002; 86: 426. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
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. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
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. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child. Fetal Neonatal Ed.
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. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Leading articles
Alpha-1 antitrypsin deficiency
R A PRIMHAK and M S TANNER
Arch. Dis. Child. 2001; 85: 2-5. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
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. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
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. [Abstract] [Full text] [PDF] [Request Permissions]  

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ADC is co-owned by the RCPCH and is the official journal of the European Academy of Paediatrics

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