Cassiman JJ - Search Results

1

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. Jehaes E, et al. Among authors: cassiman jj. Eur J Hum Genet. 2001 Mar;9(3):185-90. doi: 10.1038/sj.ejhg.5200602. Eur J Hum Genet. 2001. PMID: 11313757

2

Forensic medicine and the polymerase chain reaction technique.

Decorte R, Cassiman JJ. Decorte R, et al. Among authors: cassiman jj. J Med Genet. 1993 Aug;30(8):625-33. doi: 10.1136/jmg.30.8.625. J Med Genet. 1993. PMID: 8411046 Free PMC article. Review. No abstract available.

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. Jehaes E, et al. Among authors: cassiman jj. Eur J Hum Genet. 1998 Jul-Aug;6(4):383-95. doi: 10.1038/sj.ejhg.5200227. Eur J Hum Genet. 1998. PMID: 9781047 Free article.

4

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. Jehaes E, et al. Among authors: cassiman jj. Int J Legal Med. 2001 Dec;115(3):135-41. doi: 10.1007/s004140100221. Int J Legal Med. 2001. PMID: 11775015

5

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes.

Decorte R, Wu R, Marynen P, Cassiman JJ. Decorte R, et al. Among authors: cassiman jj. Am J Hum Genet. 1994 Mar;54(3):506-15. Am J Hum Genet. 1994. PMID: 8116620 Free PMC article.

6

Evaluation of a decontamination protocol for hair shafts before mtDNA sequencing.

Jehaes E, Gilissen A, Cassiman JJ, Decorte R. Jehaes E, et al. Among authors: cassiman jj. Forensic Sci Int. 1998 Jun 8;94(1-2):65-71. doi: 10.1016/s0379-0738(98)00052-8. Forensic Sci Int. 1998. PMID: 9670485

7

Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian families.

Cuppens H, Legius E, Cabello P, Marynen P, De Boeck C, Decorte R, Fryns JP, Eggermont E, Van den Berghe H, Cassiman JJ. Cuppens H, et al. Among authors: cassiman jj. Hum Genet. 1990 Sep;85(4):402-3. doi: 10.1007/BF02428277. Hum Genet. 1990. PMID: 2210747

8

Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).

Gu XX, Decorte R, Marynen P, Fryns JP, Cassiman JJ, Raeymaekers P. Gu XX, et al. Among authors: cassiman jj. J Med Genet. 1996 Jan;33(1):52-5. doi: 10.1136/jmg.33.1.52. J Med Genet. 1996. PMID: 8825049 Free PMC article.

9

Evaluation of the ALF DNA sequencer for high-speed sizing of short tandem repeat alleles.

Decorte R, Cassiman JJ. Decorte R, et al. Among authors: cassiman jj. Electrophoresis. 1996 Oct;17(10):1542-9. doi: 10.1002/elps.1150171007. Electrophoresis. 1996. PMID: 8957177

10

Detection of amplified VNTR alleles by direct chemiluminescence: application to the genetic identification of biological samples in forensic cases.

Decorte R, Cassiman JJ. Decorte R, et al. Among authors: cassiman jj. EXS. 1991;58:371-90. doi: 10.1007/978-3-0348-7312-3_28. EXS. 1991. PMID: 1831164 Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

439 results

Search Page