Reply to Sajantila and Budowle

Affiliations

¹ National Centre for Medical Genetics, School of Medicine & Medical Sciences, University College Dublin, Our Lady's Children's Hospital, Dublin, Ireland.
² Molecular Genetics of Rare Disorders, University Hospital of Montpellier and INSERM U827, IURC (Institut Universitaire de Recherche Clinique), Montpellier, France.
³ Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
⁴ Biomedical Quality Assurance Research Unit, Department of Human Genetics, University of Leuven, Leuven, Belgium.
⁵ Department of Paediatrics, Universitats-Kinderspital Beider Basel (UKBB), Basel, Switzerland.
⁶ Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
⁷ Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
⁸ VSOP-National Patient Alliance for Rare and Genetic Disorders, Soest, The Netherlands.
⁹ Division of Obstetrics and Gynecology, Clinical Institute of Medical Genetics, University Medical Center, Ljubljana, Slovenia.
¹⁰ Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
¹¹ Division 3 Health/Forensics, Deutsche Akkreditierungsstelle GmbH (DAkkS), Frankfurt am Main, Germany.
¹² Department of Medical Genetics, University of Pavia, Pavia, Italy.
¹³ CEQAS, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.

Comment

David E Barton et al. Eur J Hum Genet. 2016 Mar.

. 2016 Mar;24(3):330.

doi: 10.1038/ejhg.2014.290. Epub 2015 Jan 14.

¹ National Centre for Medical Genetics, School of Medicine & Medical Sciences, University College Dublin, Our Lady's Children's Hospital, Dublin, Ireland.
² Molecular Genetics of Rare Disorders, University Hospital of Montpellier and INSERM U827, IURC (Institut Universitaire de Recherche Clinique), Montpellier, France.
³ Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
⁴ Biomedical Quality Assurance Research Unit, Department of Human Genetics, University of Leuven, Leuven, Belgium.
⁵ Department of Paediatrics, Universitats-Kinderspital Beider Basel (UKBB), Basel, Switzerland.
⁶ Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.
⁷ Institute of Human Genetics, Hannover Medical School, Hannover, Germany.
⁸ VSOP-National Patient Alliance for Rare and Genetic Disorders, Soest, The Netherlands.
⁹ Division of Obstetrics and Gynecology, Clinical Institute of Medical Genetics, University Medical Center, Ljubljana, Slovenia.
¹⁰ Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
¹¹ Division 3 Health/Forensics, Deutsche Akkreditierungsstelle GmbH (DAkkS), Frankfurt am Main, Germany.
¹² Department of Medical Genetics, University of Pavia, Pavia, Italy.
¹³ CEQAS, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.

No abstract available

Comment on

Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic).
Claustres M, Kožich V, Dequeker E, Fowler B, Hehir-Kwa JY, Miller K, Oosterwijk C, Peterlin B, van Ravenswaaij-Arts C, Zimmermann U, Zuffardi O, Hastings RJ, Barton DE; European Society of Human Genetics. Claustres M, et al. Eur J Hum Genet. 2014 Feb;22(2):160-70. doi: 10.1038/ejhg.2013.125. Epub 2013 Aug 14. Eur J Hum Genet. 2014. PMID: 23942201 Free PMC article.
Postmortem medicolegal genetic diagnostics also require reporting guidance.
Sajantila A, Budowle B. Sajantila A, et al. Eur J Hum Genet. 2016 Mar;24(3):329-30. doi: 10.1038/ejhg.2014.247. Epub 2014 Dec 3. Eur J Hum Genet. 2016. PMID: 25469540 Free PMC article. No abstract available.

1. 1Sajantila A, Budowle B: Postmortem medicolegal genetic diagnostics also require reporting guidance. Eur J Hum Genet 2014, e-pub ahead of print 3 December 2014 doi:10.1038/ejhg.2014.247. - PMC - PubMed
1. 2Claustres M, Kozich V, Dequeker E et al: Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic). Eur J Hum Genet 2014; 22: 160–170. - PMC - PubMed