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pro vyhledávání: '"Soukaina Zagdan"'
Publikováno v:
The Egyptian Heart Journal, Vol 76, Iss 1, Pp 1-6 (2024)
Abstract Background Holt–Oram syndrome is a rare genetic disorder caused by a mutation in the TBX5 gene, combining skeletal and cardiac malformations. Vital prognosis depends essentially on cardiac involvement, while skeletal malformations determin
Externí odkaz:
https://doaj.org/article/55ae9808301b426f9964f7ce2b743adc