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30.05.2019 · Severity varied between individuals; while two children had mild speech delay, one child used two- to three-word sentences at age seven years ...
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A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable developmental delay and intellectual disability, movement disorder or ...
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Clinical resource with information about Gabriele de Vries syndrome and its clinical features, YY1, available genetic tests from US and labs around the ...
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01.09.2023 · Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease characterized by global development delay/intellectual disability ...
Gabriele-de Vries syndrome (GADEVS) is an autosomal dominant neurodevelopmental disorder characterized by delayed psychomotor development, ...
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“Life is not easy for any of us. But what of that? We must have perseverance and above all confidence in ourselves. We must believe that we are gifted for.
01.03.2013 · Koolen-de Vries syndrome is a disorder characterized by developmental delay and mild to moderate intellectual disability.
gabriele.de/search?hl=de Gabriele-de Vries syndrome life expectancy von www.mdpi.com
At fifteen months of age the patient was able to speak a few words, walked independently, and was able to sit on his own. Children 10 00623 g002 550. Figure 2.
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An autosomal dominant neurodevelopmental disorder characterized by delayed psychomotor development and intellectual disability. Most patients have behavioral ...
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Recently, YY1 mutations have been identified as responsible for Gabriele-DeVries syndrome (GADVES), a syndromic intellectual disability characterized by growth ...