Acanthodactylus taghitensis GENIEZ & FOUCART, 1995 https://www.lacerta.de/AS/Taxon.php?Genus=49&Species=265&Lang=eng
on phylogeographic structure and diversity were tested with generalized linear models
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Acanthodactylus dumerili (MILNE-EDWARDS, 1829) https://www.lacerta.de/AS/Taxon.php?Genus=49&Species=241
on phylogeographic structure and diversity were tested with generalized linear models
Acanthodactylus longipes BOULENGER, 1918 https://www.lacerta.de/AS/Taxon.php?Genus=49&Species=249&Lang=eng
on phylogeographic structure and diversity were tested with generalized linear models
Acanthodactylus scutellatus (AUDOUIN, 1809) https://www.lacerta.de/AS/Taxon.php?Genus=49&Species=262&Lang=ger
on phylogeographic structure and diversity were tested with generalized linear models
Acanthodactylus scutellatus (AUDOUIN, 1809) https://www.lacerta.de/AS/Taxon.php?Genus=49&Species=262
on phylogeographic structure and diversity were tested with generalized linear models
Mesalina bernoullii (SCHENKEL, 1901) https://www.lacerta.de/AS/Taxon.php?Genus=51&Species=362&Lang=ger
Species distribution models of the four species show that the areas of suitable habitat
Mesalina bernoullii (SCHENKEL, 1901) https://www.lacerta.de/AS/Taxon.php?Genus=51&Species=362
Species distribution models of the four species show that the areas of suitable habitat
Mesalina saudiarabica MORAVEC et al., 2017 https://www.lacerta.de/AS/Taxon.php?Genus=51&Species=361
Species distribution models of the four species show that the areas of suitable habitat
Mesalina microlepis (ANGEL, 1936) https://www.lacerta.de/AS/Taxon.php?Genus=51&Species=363&Lang=ger
Species distribution models of the four species show that the areas of suitable habitat
Congolacerta vauereselli – bibliography https://www.lacerta.de/AS/Bibliografie.php?Genus=54&Species=325&Taxon=1
phylogenetic-comparative approach was used to assess and refine existing secondary structure models