Vocal imitation in human infants and in some orders of birds relies on auditory-guided motor
learning during a sensitive period of development. It proceeds from'babbling'(in humans) …

Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome
characterized by impaired speech development and linguistic deficits. Recent genomic …

Reference-quality genomes are expected to provide a resource for studying gene structure,
function, and evolution. However, often genes of interest are not completely or accurately …

Rhododendron delavayi Franch. is globally famous as an ornamental plant. Its distribution in
southwest China covers several different habitats and environments. However, not much …

For over 50 years, the great tit (Parus major) has been a model species for research in
evolutionary, ecological and behavioural research; in particular, learning and cognition have …

The gene encoding the forkhead box transcription factor, FOXP2, is essential for developing
the full articulatory power of human language. Mutations of FOXP2 cause developmental …

Neuroconstructivism is a theoretical framework focusing on the construction of
representations in the developing brain. Cognitive development is explained as emerging …

Новая книга Александра Маркова-это увлекательный рассказ о происхождении и
устройстве человека, основанный на последних исследованиях в антропологии …

The most well-described example of an inherited speech and language disorder is that
observed in the multigenerational KE family, caused by a heterozygous missense mutation …

Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the
only known cause of developmental speech and language disorders in humans. To date …