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Ugeskrift for Laeger|April 12, 2017
[Mayer-Rokitansky-Küster-Hauser syndrome]Morten Herlin, Michael Bjørn Petersen
Orphanet Journal of Rare Diseases|August 22, 2020
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive updateMorten Krogh Herlin, Michael Bjørn Petersen, Mats Brännström
Human Reproduction (Oxford, England)|September 10, 2016
Prevalence and patient characteristics of Mayer-Rokitansky-Küster-Hauser syndrome: a nationwide registry-based studyMorten Herlin, Anne-Mette Bay Bjørn, Maria Rasmussen, et al.
Fertility and Sterility|September 11, 2018
Treatment of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome in Denmark: a nationwide comparative study of anatomical outcome and complicationsMorten Herlin, Anne-Mette Bay Bjørn, Laura Krogh Jørgensen, et al.
Molecular Genetics & Genomic Medicine|March 5, 2021
First reported CABP2-related non-syndromic hearing loss in Northern EuropeInger Norlyk Sheyanth, Allan Thomas Højland, Henrik Okkels, et al.
Molecular Genetics & Genomic Medicine|March 10, 2021
First reported case of Doyne honeycomb retinal dystrophy (Malattia Leventinese/autosomal dominant drusen) in ScandinaviaInger Norlyk Sheyanth, Ihab Bishara Lolas, Henrik Okkels, et al.
Ugeskrift for Laeger|April 7, 2018
[Preimplantation genetic diagnosis]Hans Jakob Ingerslev, Birte Degn, Christina Hnida, et al.
European Journal of Medical Genetics|August 27, 2019
Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndromeHelena Gásdal Karstensen, Nanna Dahl Rendtorff, Lone Sandbjerg Hindbæk, et al.
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