Literature DB >> 31274184

Meier-Gorlin syndrome caused by ORC1 mutation associated with chromosomal breakage - coincidental finding or new feature of known syndrome?

Jarmila Vojtková1, Miriam Čiljaková2, Miloš Jeseňák2, Peter Bánovčin2.   

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Year:  2019        PMID： 31274184     DOI： 10.5603/EP.a2019.0032

Source DB:  PubMed          Journal:  Endokrynol Pol        ISSN： 0423-104X            Impact factor:   1.582


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  2 in total

Review 1.  Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms.

Authors:  Megan Schmit; Anja-Katrin Bielinsky
Journal:  Int J Mol Sci       Date:  2021-01-18       Impact factor: 5.923

2.  Meier-Gorlin syndrome with prenatal ultrasound findings and successful growth hormone therapy: Six years follow-up of a rare case.

Authors:  Rahim Vakili; Moein Mobini; Farbod Hatami; Saba Vakili; Niloufar Valizadeh
Journal:  Radiol Case Rep       Date:  2022-03-04
  2 in total

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