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 1-10 of 59 total displayed.

Leading articles
With new prenatal testing, will babies with Down syndrome slowly disappear?

Brian G Skotko
Arch. Dis. Child. 2009 94: 823 -826; published online before print as 10.1136/adc.2009.166017 [Extract] [Full text] [PDF] [Request Permissions]  

Perspectives
Food for thought: autophagic vacuolar myopathies

E-M Strehle
Arch. Dis. Child. 2009; 94: 567-569. [Extract] [Full text] [PDF] [Request Permissions]  

Short reports
Interleukin-6 G(–174)C polymorphism is associated with mental retardation in cystic periventricular leucomalacia in preterm infants

B Resch, A Radinger, C Mannhalter, A Binder, J Haas, and W D Müller
Arch. Dis. Child. Fetal Neonatal Ed. 2009 94: F304 -F306; published online before print as 10.1136/adc.2008.140244 [Abstract] [Full text] [PDF] [Request Permissions]  

Review
Hyperinsulinaemic hypoglycaemia

R R Kapoor, S E Flanagan, C James, J Shield, S Ellard, and K Hussain
Arch. Dis. Child. 2009 94: 450 -457; published online before print as 10.1136/adc.2008.148171 [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Cytokine gene polymorphisms in preterm infants with necrotising enterocolitis: genetic association study

G Henderson, S Craig, R J Baier, N Helps, P Brocklehurst, and W McGuire
Arch. Dis. Child. Fetal Neonatal Ed. 2009 94: F124 -F128; published online before print as 10.1136/adc.2007.119933 [Abstract] [Full text] [PDF] [Request Permissions]  

Case reports
Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation

N-C Lee, D Dimmock, W-L Hwu, L-Y Tang, W-C Huang, A C Chinault, and L-J C Wong
Arch. Dis. Child. 2009; 94: 55-58. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Interleukin-6 (–174C) polymorphism and the risk of sepsis in very low birth weight infants: meta-analysis

M Chauhan and W McGuire
Arch. Dis. Child. Fetal Neonatal Ed. 2008 93: F427 -F429; published online before print as 10.1136/adc.2007.134205 [Abstract] [Full text] [PDF] [Request Permissions]  

Perspectives
Challenges in the genetic testing of children for familial cancers

Angus J Clarke and Clara Gaff
Arch. Dis. Child. 2008; 93: 911-914. [Extract] [Full text] [PDF] [Request Permissions]  

Leading articles
Tuberous sclerosis—what’s new?

John P Osborne, Jane Merrifield, and Finbar J K O’Callaghan
Arch. Dis. Child. 2008 93: 728 -731; published online before print as 10.1136/adc.2006.094938 [Extract] [Full text] [PDF] [Request Permissions]  

Original articles
Association between birth weight and adolescent systolic blood pressure in a caucasian birth cohort differs according to skin type, CRH promoter or 11β-HSD2 genotype

T Dwyer, L Blizzard, B Patterson, A-L Ponsonby, K Martin, S Quinn, M M Sale, S M Richards, R Morley, S Rich, and J L Dickinson
Arch. Dis. Child. 2008 93: 760 -767; published online before print as 10.1136/adc.2007.129122 [Abstract] [Full text] [PDF] [Request Permissions]