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Author/Creator Goossens, Remko

2. Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy. (9th June 2020)

Authors:
Hamanaka, Kohei; Šikrová, Darina; Mitsuhashi, Satomi; Masuda, Hiroki; Sekiguchi, Yukari; Sugiyama, Atsuhiko; Shibuya, Kazumoto; Lemmers, Richard J.L.F.; Goossens, Remko; Ogawa, Megumu; Nagao, Koji; Obuse, Chikashi; Noguchi, Satoru; Hayashi, Yukiko K.; Kuwabara, Satoshi; Balog, Judit; Nishino, Ich...
Journal:
Neurology
Issue:
Volume 94:Number 23(2020)
Page Start:
Record Type:
Journal Article
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3. Intronic SMCHD1 variants in FSHD: testing the potential for CRISPR-Cas9 genome editing. Issue 12 (1st November 2019)

Authors:
Goossens, Remko; van den Boogaard, Marlinde L; Lemmers, Richard J L F; Balog, Judit; van der Vliet, Patrick J; Willemsen, Iris M; Schouten, Julie; Maggio, Ignazio; van der Stoep, Nienke; Hoeben, Rob C; Tapscott, Stephen J; Geijsen, Niels; Gonçalves, Manuel A F V; Sacconi, Sabrina; Tawil, Rabi; va...
Journal:
Journal of medical genetics
Issue:
Volume 56:Issue 12(2019)
Page Start:
828
Record Type:
Journal Article
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4. Monosomy 18p is a risk factor for facioscapulohumeral dystrophy. Issue 7 (21st March 2018)

Authors:
Balog, Judit; Goossens, Remko; Lemmers, Richard J L F; Straasheijm, Kirsten R; van der Vliet, Patrick J; Heuvel, Anita van den; Cambieri, Chiara; Capet, Nicolas; Feasson, Léonard; Manel, Veronique; Contet, Julian; Kriek, Marjolein; Donlin-Smith, Colleen M; Ruivenkamp, Claudia A L; Heard, Patricia...
Journal:
Journal of medical genetics
Issue:
Volume 55:Issue 7(2018)
Page Start:
469
Record Type:
Journal Article
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