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Items: 1 to 20 of 103

1.

Genetic analysis of the presumptive blood from Louis XVI, King of France.

Lalueza-Fox C, Gigli E, Bini C, Calafell F, Luiselli D, Pelotti S, Pettener D.

Forensic Sci Int Genet. 2011 Nov;5(5):459-63. doi: 10.1016/j.fsigen.2010.09.007. Epub 2010 Oct 10.

PMID:
20940110
2.

Genetic comparison of the head of Henri IV and the presumptive blood from Louis XVI (both Kings of France).

Charlier P, Olalde I, Solé N, Ramírez O, Babelon JP, Galland B, Calafell F, Lalueza-Fox C.

Forensic Sci Int. 2013 Mar 10;226(1-3):38-40. doi: 10.1016/j.forsciint.2012.11.018. Epub 2012 Dec 30.

PMID:
23283403
3.

Mitochondrial DNA analysis on remains of a putative son of Louis XVI, King of France and Marie-Antoinette.

Jehaes E, Decorte R, Peneau A, Petrie JH, Boiry PA, Gilissen A, Moisan JP, Van den Berghe H, Pascal O, Cassiman JJ.

Eur J Hum Genet. 1998 Jul-Aug;6(4):383-95.

4.

Genomic analysis of the blood attributed to Louis XVI (1754-1793), king of France.

Olalde I, Sánchez-Quinto F, Datta D, Marigorta UM, Chiang CW, Rodríguez JA, Fernández-Callejo M, González I, Montfort M, Matas-Lalueza L, Civit S, Luiselli D, Charlier P, Pettener D, Ramírez O, Navarro A, Himmelbauer H, Marquès-Bonet T, Lalueza-Fox C.

Sci Rep. 2014 Apr 24;4:4666. doi: 10.1038/srep04666.

5.

Mitochondrial DNA analysis of the putative heart of Louis XVII, son of Louis XVI and Marie-Antoinette.

Jehaes E, Pfeiffer H, Toprak K, Decorte R, Brinkmann B, Cassiman JJ.

Eur J Hum Genet. 2001 Mar;9(3):185-90.

7.

Genetic genealogy reveals true Y haplogroup of House of Bourbon contradicting recent identification of the presumed remains of two French Kings.

Larmuseau MH, Delorme P, Germain P, Vanderheyden N, Gilissen A, Van Geystelen A, Cassiman JJ, Decorte R.

Eur J Hum Genet. 2014 May;22(5):681-7. doi: 10.1038/ejhg.2013.211. Epub 2013 Oct 9.

8.

Pitfalls in the analysis of mitochondrial DNA from ancient specimens and the consequences for forensic DNA analysis: the historical case of the putative heart of Louis XVII.

Jehaes E, Toprak K, Vanderheyden N, Pfeiffer H, Cassiman JJ, Brinkmann B, Decorte R.

Int J Legal Med. 2001 Dec;115(3):135-41.

PMID:
11775015
9.

Genetic differentiation in pointing dog breeds inferred from microsatellites and mitochondrial DNA sequence.

Parra D, Méndez S, Cañón J, Dunner S.

Anim Genet. 2008 Feb;39(1):1-7. doi: 10.1111/j.1365-2052.2007.01658.x.

PMID:
18254732
10.

Utility of Y-STR haplotype and mtDNA sequence in personal identification of human remains.

Koyama H, Iwasa M, Tsuchimochi T, Maeno Y, Isobe I, Matsumoto T, Nagao M.

Am J Forensic Med Pathol. 2002 Jun;23(2):181-5.

PMID:
12040265
11.

Portrait of the 'Temple Child', a missing-link in the case of Louis XVII.

Puech PF.

Int J Legal Med. 1995;107(4):209-12.

PMID:
7599099
12.

The population history of the Xibe in northern China: a comparison of autosomal, mtDNA and Y-chromosomal analyses of migration and gene flow.

Powell GT, Yang H, Tyler-Smith C, Xue Y.

Forensic Sci Int Genet. 2007 Jun;1(2):115-9. doi: 10.1016/j.fsigen.2007.01.015. Epub 2007 Feb 27.

PMID:
19083740
13.

[Genetic analysis of the putative remains of general Władysław Sikorski].

Kupiec T, Branicki W.

Arch Med Sadowej Kryminol. 2009 Jan-Mar;59(1):9-14. Polish.

PMID:
19711812
14.

A genetic investigation of Korean mummies from the Joseon Dynasty.

Kim NY, Lee HY, Park MJ, Yang WI, Shin KJ.

Mol Biol Rep. 2011 Jan;38(1):115-21. doi: 10.1007/s11033-010-0084-4. Epub 2010 Mar 21.

PMID:
20306303
15.

LOUIS XIV, THE SUN KING, OVERSHADOWED BY MEDICAL PRACTICE.

SEIDLER E.

Medico (Int). 1964;39:17-23. No abstract available.

PMID:
14163177
16.

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.

Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H.

Am J Hum Genet. 2005 Aug;77(2):280-96. Epub 2005 Jul 6.

17.

A case of personal identification due to detection of rare DNA types from seminal stain.

Tsutsumi H, Komuro T, Mukoyama R, Izawa H, Tie J, Uchigasaki S.

J Oral Sci. 2009 Dec;51(4):645-50.

18.

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.

Sturm RA, Duffy DL, Zhao ZZ, Leite FP, Stark MS, Hayward NK, Martin NG, Montgomery GW.

Am J Hum Genet. 2008 Feb;82(2):424-31. doi: 10.1016/j.ajhg.2007.11.005. Epub 2008 Jan 24.

19.

Human eye colour and HERC2, OCA2 and MATP.

Mengel-From J, Børsting C, Sanchez JJ, Eiberg H, Morling N.

Forensic Sci Int Genet. 2010 Oct;4(5):323-8. doi: 10.1016/j.fsigen.2009.12.004. Epub 2010 Jan 12.

PMID:
20457063
20.

Apparent intrachromosomal exchange on the human Y chromosome explained by population history.

Kittler R, Erler A, Brauer S, Stoneking M, Kayser M.

Eur J Hum Genet. 2003 Apr;11(4):304-14.

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