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That rate is similar, for example, to the rate of fragile-X syndrome, which is the second-most-common type of congenital learning difficulty after Down's syndrome.
We find that congenital learning and interorganizational learning lead to increased behavioural additionality.
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(2012) showed that as with the operant judgement bias task (Enkel et al., 2010), a congenital learned helplessness rat strain exhibited a pessimistic judgement bias.
Additionally, in a congenital learned helpless rat strain performing the same task, a shift in responding away from obtaining reward and towards increased avoidance of punishment was observed (Enkel et al., 2010).
Expressed in both heart and brain, MED13L is associated with early development of both heart and brain since its missense mutations and gene interruption are found in patients with congenital heart defect, learning disabilities, and facial anomalies (Muncke et al. 2003; Asadollahi et al. 2013; Davis et al. 2013).
42 For patients with schizophrenia, a clinician today should be armed with a high index of suspicion for 22q11.2DS and/or consistently use established clinical screening criteria to detect features suggesting this genetic diagnosis, such as dysmorphic facies, a nasal voice, congenital anomalies, and/or learning difficulties.
The 22q11.2DS phenotype is highly variable with features including velopharyngeal insufficiency, congenital cardiac defects and learning difficulties.
As we later learned, congenital heart problems are the most common type of birth defect in the United States.
About a year later, Nathan-Neil (pronounced Nathaniel) was born with a lung infection and DiGeorge syndrome, a disorder caused by a chromosomal defect that can result in congenital heart disease, skeletal abnormalities, learning difficulties and other problems.
The phenotype of the 22q11.21 duplication is extremely variable, ranging from normal to learning disability to congenital defects but not associated with peripheral nerve disease [ 57].
The UK10K project was a collaborative project that brought together researchers working on obesity, autism, schizophrenia, familial hypercholesterolemia, thyroid disorders, learning disabilities, ciliopathies, congenital heart disease, coloboma, neuromuscular disorders, and rare disorders including severe insulin resistance.
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