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Molecular genetics

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 59 total displayed.

Past content
Arch. Dis. Child. Fetal Neonatal Ed.
Images in neonatal medicine
Congenital hyperinsulinism: [18F]DOPA PET/CT scan of a focal lesion in the head of the pancreas
R R Kapoor, C Gilbert, K Mohnike, O Blankenstein, F Fuechtner, and K Hussain
Arch. Dis. Child. Fetal Neonatal Ed. 2008; 93: F166. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Perspectives
Hyperinsulinaemic hypoglycaemia: biochemical basis and the importance of maintaining normoglycaemia during management
Khalid Hussain, Oliver Blankenstein, Pascale De Lonlay, and Henrik T Christesen
Arch. Dis. Child. 2007; 92: 568-570. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child. Fetal Neonatal Ed.
Original articles
Cognitive outcome and cyclo-oxygenase-2 gene (–765 G/C) variation in the preterm infant
D R Harding, S E Humphries, A Whitelaw, N Marlow, and H E Montgomery
Arch. Dis. Child. Fetal Neonatal Ed. 2007 92: F108 -F112; published online before print as 10.1136/adc.2006.099499 [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child. Fetal Neonatal Ed.
Original articles
Association of interferon {gamma} T+874A and interleukin 12 p40 promoter CTCTAA/GC polymorphism with the need for respiratory support and perinatal complications in low birthweight neonates
G Bokodi, L Derzbach, I Bányász, T Tulassay, and B Vásárhelyi
Arch. Dis. Child. Fetal Neonatal Ed. 2007 92: F25 -F29; published online before print as 10.1136/adc.2005.086421 [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Perspectives
Frequency of metabolic disorders: more than one needle in the haystack
P J Lee and P Cook
Arch. Dis. Child. 2006; 91: 879-880. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Original articles
Markedly elevated neonatal immunoreactive trypsinogen levels in the absence of cystic fibrosis gene mutations is not an indication for further testing
J Massie, L Curnow, N Tzanakos, I Francis, and C F Robertson
Arch. Dis. Child. 2006 91: 222 -225; published online before print as 10.1136/adc.2005.081349 [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Short reports
Clinical and molecular findings in IPEX syndrome
A K Myers, L Perroni, C Costigan, and W Reardon
Arch. Dis. Child. 2006; 91: 63-64. [Abstract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Perspectives
A monogenetic disorder yet multiple and varied clinical manifestations
L I Landau
Arch. Dis. Child. 2005; 90: 992-993. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child. Ed. Pract.
BEST PRACTICE
Helicobacter pylori infection in paediatric practice
D I Campbell and J E Thomas
Arch. Dis. Child. Ed. Pract. 2005; 90: ep25-30ep. [Extract] [Full text] [PDF] [Request Permissions]  

Arch. Dis. Child.
Community child health, public health, and epidemiology
The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants
M Mei-Zahav, P Durie, J Zielenski, M Solomon, E Tullis, L-C Tsui, and M Corey
Arch. Dis. Child. 2005; 90: 675-679. [Abstract] [Full text] [PDF] [Request Permissions]  

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