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Gene diagnostics of the Aper syndrome

Average price: ≈160.6€
It is treated in 151 clinic
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Gene diagnostics of the Aper syndrome

Description

 Генодиагностика синдрома Апера - это молекулярно-генетическое исследование гена рецептора-2 фактора роста фибробластов (FGFR2). Ген расположен на хромосоме 10q26. Наиболее частые мутации FGFR2 при этом заболевании обнаруживаются в седьмом экзоне. Возможна антенатальная диагностика синдрома Апера. Мутации FGFR2 также приводят к развитию ряда других заболеваний, связанных с черепно-лицевыми аномалиями скелета.
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