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pro vyhledávání: '"Ghazaleh Aldaghi"'
Autor:
Shahin Koomanaee, Setila Dalili, Seyyedeh Azade Hoseini Nouri, Seyedeh Zohreh Jalali, Manijeh Tabrizi, Ghazaleh Aldaghi, Afagh Hassanzadeh Rad
Publikováno v:
Acta Medica Iranica, Vol 60, Iss 9 (2022)
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder with homozygous or heterozygous mutations in one of the five following genes (ORC1, ORC4, ORC6, CDT1, and CDC6). This syndrome is characterized by the triad of short stature (pre/post
Externí odkaz:
https://doaj.org/article/c19c7dd67ee945e3b31aea0b7d348cca
