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1. Historical human remains identification through maternal and paternal genetic signatures in a founder population with extensive genealogical record. Issue 4 (16th February 2020)

2. Mutations in TMEM231 cause Joubert syndrome in French Canadians. Issue 10 (25th September 2012)

3. Disruption of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria. Issue 5 (3rd February 2015)

4. Genome diversity in the Neolithic Globular Amphorae culture and the spread of Indo-European languages. Issue 1867 (22nd November 2017)

5. Back Cover, Volume 40, Issue 8. Issue 8 (9th August 2019)

6. Molecular characterization of a large group of Mucopolysaccharidosis type IIIC patients reveals the evolutionary history of the disease. Issue 8 (22nd June 2019)