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Genetic screening / counselling
Contributing journals to this collection:
Archives of Disease in Childhood - Education and Practice
and Archives of Disease in Childhood - Fetal and Neonatal Edition
Citations 1-7 of 7 total displayed.
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Guideline review
Hypercholesterolaemia in children guidelines review
- J H Baumer and J P H Shield
Arch. Dis. Child. Ed. Pract. 2009; 94: 84-86.
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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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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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Controversy
Antenatal treatment of a mother bearing a fetus with congenital adrenal hyperplasia
- C G D Brook;, IEUAN HUGHES;, and CHRISTOPHER J H KELNAR
Arch. Dis. Child. Fetal Neonatal Ed. 2000; 82: F176-F181.
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Original articles
Perinatal cortical infarction within middle cerebral artery trunks
- Paul Govaert, Erika Matthys, Alexandra Zecic, Filip Roelens, Ann Oostra, and Bart Vanzieleghem
Arch. Dis. Child. Fetal Neonatal Ed. 2000; 82: F59-F63.
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Original articles
HFE gene mutation and transferrin saturation in very low birthweight infants
- Rolf F Maier, Heiko Witt, Christoph Bührer, Eberhard Mönch, and Eckart Köttgen
Arch. Dis. Child. Fetal Neonatal Ed. 1999; 81: F144-F145.
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Original articles
Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly
- Otfried Debus, Hans Georg Koch, Gerhard Kurlemann, Ronald Sträter, Heinrich Vielhaber, Peter Weber, and Ulrike Nowak-Göttl
Arch. Dis. Child. Fetal Neonatal Ed. 1998; 78: F121-F124.
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