Výsledky vyhledávání - "María C. Gonzalez-Gonzalez"

Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females

Autor: Oscar F. Chacon-Camacho, Alan Martinez-Aguilar, Alejandro Navas-Perez, Rocio Arce-Gonzalez, María C. Gonzalez-Gonzalez, Juan Carlos Zenteno

Publikováno v: Ophthalmic Genetics. 43:224-229

PURPOSE X-linked megalocornea (XMC) is a rare anterior segment malformation characterized by a nonprogressive enlargement of the cornea to 13 mm or greater in the setting of normal intraocular pressure. XMC is caused by mutations in the CHRDL1 gene a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6d4cae85c5f36723ce1eb950a60b2ebe
https://doi.org/10.1080/13816810.2021.2002917

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Novel

Autor: Rocio, Arce-Gonzalez, Oscar F, Chacon-Camacho, Alejandro, Navas-Perez, María C, Gonzalez-Gonzalez, Alan, Martinez-Aguilar, Juan Carlos, Zenteno

Publikováno v: Ophthalmic genetics. 43(2)

X-linked megalocornea (XMC) is a rare anterior segment malformation characterized by a nonprogressive enlargement of the cornea to 13 mm or greater in the setting of normal intraocular pressure. XMC is caused by mutations in theThree subjects (a fath

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::24ec0e38f37e4e1c75b5924734369258
https://pubmed.ncbi.nlm.nih.gov/34844512

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