O'Callaghan, Michael E <br/><br/>
Fetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study.  [electronic resource] 

 -  Pediatrics  Feb 2012 
 - e414-23 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-4275 
<br/><br/><label>Standard No.: </label>10.1542/peds.2011-0739  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Apolipoproteins E--genetics<br/>Australia<br/>Case-Control Studies<br/>Cerebral Palsy--epidemiology<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Association Studies<br/>Genetic Carrier Screening<br/>Genetic Predisposition to Disease--genetics<br/>Haplotypes--genetics<br/>Humans<br/>Infant, Newborn<br/>Mannose-Binding Lectin--genetics<br/>Phenotype<br/>Polymorphism, Single Nucleotide--genetics<br/>Pregnancy<br/>Prothrombin--genetics