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Forensic Science International|September 24, 2002
Sequence variation and allele nomenclature for the X-linked STRs DXS9895, DXS8378, DXS7132, DXS6800, DXS7133, GATA172D05, DXS7423 and DXS8377Jeanett Edelmann, Danilo Deichsel, Sandra Hering, et al.
International Journal of Legal Medicine|February 21, 2009
Validation of six closely linked STRs located in the chromosome X centromere regionJeanett Edelmann, Sandra Hering, Christa Augustin, et al.
International Journal of Legal Medicine|November 26, 2009
X chromosomal recombination--a family study analysing 39 STR markers in German three-generation pedigreesSandra Hering, Jeanett Edelmann, Christa Augustin, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|November 16, 2006
Compound heterozygous mutations of the SBDS gene in a patient with Shwachman-Diamond syndrome, type 1 diabetes mellitus and osteoporosisJonas Rosendahl, Niels Teich, Joachim Mossner, et al.
International Journal of Legal Medicine|July 20, 2011
Long QT syndrome mutation detection by SNaPshot techniqueJeanett Edelmann, Stefanie Schumann, Marina Nastainczyk, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|March 5, 2008
Adenoid squamous carcinoma (pseudoangiosarcomatous carcinoma) of the vulva: a rare but highly aggressive variant of squamous cell carcinoma-report of a case and review of the literatureLars-Christian Horn, Uwe G Liebert, Jeanett Edelmann, et al.
International Journal of Legal Medicine|August 9, 2008
The STR cluster DXS10148-DXS8378-DXS10135 provides a powerful tool for X-chromosomal haplotyping at Xp22Tanja Hundertmark, Sandra Hering, Jeanett Edelmann, et al.
International Journal of Legal Medicine|February 3, 2007
Complex variability of intron 40 of the von Willebrand factor (vWF) geneSandra Hering, Christa Augustin, Jeanett Edelmann, et al.
International Journal of Legal Medicine|August 13, 2005
Haplotyping of STR cluster DXS6801-DXS6809-DXS6789 on Xq21 provides a powerful tool for kinship testingReinhard Szibor, Sandra Hering, Eberhard Kuhlisch, et al.
International Journal of Legal Medicine|December 14, 2005
DXS10079, DXS10074 and DXS10075 are STRs located within a 280-kb region of Xq12 and provide stable haplotypes useful for complex kinship casesSandra Hering, Christa Augustin, Jeanett Edelmann, et al.
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