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American Journal of Human Genetics|September 8, 2009
FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndromeAnas M Alazami, Ranad Shaheen, Fatema Alzahrani, et al.International Journal of Legal Medicine|July 14, 2005
Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic studyHorst Wedekind, Thomas Bajanowski, Patrick Friederich, et al.International Journal of Legal Medicine|February 28, 2008
Novel transcript profiling of diffuse alveolar damage induced by hyperoxia exposure in mice: normalization by glyceraldehyde 3-phosphate dehydrogenaseIchiroh Shimada, Kazuhiro Matsui, Bernd Brinkmann, et al.Pediatrics|June 4, 2008
Head covering and the risk for SIDS: findings from the New Zealand and German SIDS case-control studiesEdwin A Mitchell, John M D Thompson, David M O Becroft, et al.International Journal of Legal Medicine|October 26, 2007
Mitochondrial control region sequences from a Vietnamese population sampleJodi A Irwin, Jessica L Saunier, Katherine M Strouss, et al.International Journal of Legal Medicine|November 10, 2011
Cytokines and sudden infant deathMechtild M T Vennemann, Brigitte Loddenkötter, Tony Fracasso, et al.Iscience|September 9, 2024
Kaspar Hauser's alleged noble origin - New molecular genetic analyses resolve the controversyWalther Parson, Christina Amory, Turi King, et al.Forensic Science International|March 26, 2004
The EDNAP mitochondrial DNA population database (EMPOP) collaborative exercises: organisation, results and perspectivesWalther Parson, Anita Brandstätter, Antonio Alonso, et al.Forensic Science International. Genetics|December 17, 2008
Identification of West Eurasian mitochondrial haplogroups by mtDNA SNP screening: results of the 2006-2007 EDNAP collaborative exerciseWalther Parson, Liane Fendt, David Ballard, et al.International Journal of Legal Medicine|February 6, 2010
Petechial bleedings in sudden infant deathTony Fracasso, Mechtild Vennemann, Mirjam Klöcker, et al.Pageof 5