- ►luc.edu [PDF] TA Thornton-Wells, JH Moore, JL Haines - TRENDS in Genetics, 2004 - Elsevier Molecular biologists and geneticists alike now acknowledge that most common
human diseases with a genetic component are likely to have complex etiologies.
Yet despite this belief, many statistical geneticists continue applying, in ... Cited by 135 - Related articles - All 6 versions
R Padmanabhan - Congenital anomalies, 2006 - rc.kfshrc.edu.sa Correspondence: Rengasamy Padmanabhan, MS, PhD, Cbiol, FIBiol (Lond), DSc (med),
Department of Anatomy, Faculty of Medicine and Health Sciences, UAE University,
PO Box 17666, Al Ain, United Arab Emirates. Email: padmanabhanr@uaeu.ac.ae ... Cited by 49 - Related articles - View as HTML - BL Direct - All 8 versions
GY Zou, A Donner - Ann Hum Genet, 2006 - interscience.wiley.com Testing for departures from the assumption of Hardy-Weinberg equilibrium (HWE)
has been widely recommended as a preliminary step in the analysis of genetic
case-control studies. Some authors suggest using a two-stage procedure in ... Cited by 45 - Related articles - BL Direct - All 3 versions
RM Cabrera, DS Hill, AJ Etheredge, RH … - Birth Defects Research Part C Embryo Today Reviews, 2004 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 30 - Related articles - All 3 versions
IJM van der Linden, M den Heijer, LA Afman, … - Journal of Molecular Medicine, 2006 - Springer Page 1. ORIGINAL ARTICLE The methionine synthase reductase 66A>G polymorphism
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IJM van der Linden, LA Afman, SG Heil, HJ … - Proceedings of the Nutrition Society, 2007 - Cambridge Univ Press Page 1. A meeting hosted by the Irish Section of the Nutrition Society
was held at Queen's University Belfast on 15–17 June 2005 ... Cited by 24 - Related articles - BL Direct - All 10 versions
VM Whitehead… - Br J Haematol, 2006 - rc.kfshrc.edu.sa Cobalamin deficiency in the newborn usually results from cobalamin deficiency in
the mother. Megaloblastic anaemia, pancytopenia and failure to thrive can be
present, accompan- ied by neurological deficits if the diagnosis is ... Cited by 23 - Related articles - View as HTML - BL Direct - All 6 versions
AE Beaudin, PJ Stover - BIRTH DEFECTS RESEARCH PART C EMBRYO …, 2007 - interscience.wiley.com Neural tube defects (NTDs) refer to a cluster of neurodevelopmental conditions
associated with failure of neural tube closure during embryonic development.
Worldwide prevalence of NTDs ranges from approximately 0.5 to 60 per 10,000 ... Cited by 19 - Related articles - BL Direct - All 2 versions
- ►nih.gov CL Elmore, X Wu, D Leclerc, ED Watson, T … - Molecular genetics and metabolism, 2007 - Elsevier Hyperhomocyst(e)inemia is a metabolic derangement that is linked to the
distribution of folate pools, which provide one-carbon units for biosynthesis of
purines and thymidylate and for remethylation of homocysteine to form ... Cited by 20 - Related articles - All 4 versions