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Mariëlle Wohlgemuth

Showing results (1-10 of 4) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|August 23, 2011
[Ocular myasthenia gravis: diagnosis often delayed]Bianca van den Berg, Mariëlle Wohlgemuth, Cees C Tijssen
American Journal of Human Genetics|October 7, 2004
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophyRichard J F L Lemmers, Mariëlle Wohlgemuth, Rune R Frants, et al.
Neurology|July 13, 2018
A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1Mariëlle Wohlgemuth, Richard J Lemmers, Marianne Jonker, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral DystrophyMarlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Nederlands Tijdschrift Voor Geneeskunde|August 23, 2011
[Ocular myasthenia gravis: diagnosis often delayed]Bianca van den Berg, Mariëlle Wohlgemuth, Cees C Tijssen
American Journal of Human Genetics|October 7, 2004
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophyRichard J F L Lemmers, Mariëlle Wohlgemuth, Rune R Frants, et al.
Neurology|July 13, 2018
A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1Mariëlle Wohlgemuth, Richard J Lemmers, Marianne Jonker, et al.
American Journal of Human Genetics|May 7, 2016
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral DystrophyMarlinde L van den Boogaard, Richard J L F Lemmers, Judit Balog, et al.
Pageof 1