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Search Results - Hartel, Bas P
Search Results - Hartel, Bas P
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Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation
by
Slijkerman, Radulfus WN
,
Vaché, Christel
,
Dona, Margo
,
García-García, Gema
,
Claustres, Mireille
,
Hetterschijt, Lisette
,
Peters, Theo A
,
Hartel, Bas P
,
Pennings, Ronald JE
,
Millan, José M
,
Aller, Elena
,
Garanto, Alejandro
,
Collin, Rob WJ
,
Kremer, Hannie
,
Roux, Anne-Françoise
,
Van Wijk, Erwin
Published in
Molecular therapy. Nucleic acids
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A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa
by
Hartel, Bas P.
,
Löfgren, Maria
,
Huygen, Patrick L.M.
,
Guchelaar, Iris
,
Lo-A-Njoe Kort, Nicole
,
Sadeghi, Andre M.
,
van Wijk, Erwin
,
Tranebjærg, Lisbeth
,
Kremer, Hannie
,
Kimberling, William J.
,
Cremers, Cor W.R.J.
,
Möller, Claes
,
Pennings, Ronald J.E.
Published in
Hearing research
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Comparative study of total shoulder arthroplasty versus total shoulder surface replacement for glenohumeral osteoarthritis with minimum 2-year follow-up
by
Kooistra, Bauke W., MD, PhD
,
Willems, W. Jaap, MD,PhD
,
Lemmens, Eelke, MSc
,
Hartel, Bas P., MD
,
van den Bekerom, Michel P.J., MD
,
van Deurzen, Derek F.P., MD
Published in
Journal of shoulder and elbow surgery
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MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse
by
Wesdorp, Mieke
,
Murillo-Cuesta, Silvia
,
Peters, Theo
,
Celaya, Adelaida M.
,
Oonk, Anne
,
Schraders, Margit
,
Oostrik, Jaap
,
Gomez-Rosas, Elena
,
Beynon, Andy J.
,
Hartel, Bas P.
,
Okkersen, Kees
,
Koenen, Hans J.P.M.
,
Weeda, Jack
,
Lelieveld, Stefan
,
Voermans, Nicol C.
,
Joosten, Irma
,
Hoyng, Carel B.
,
Lichtner, Peter
,
Kunst, Henricus P.M.
,
Feenstra, Ilse
,
de Bruijn, Suzanne E.
,
van Dooren, M.F.
,
de Gier, H.H.W.
,
Hoefsloot, E.H.
,
van der Schroeff, M.P.
,
Kant, S.G.
,
Rotteveel, L.J.C.
,
Frints, S.G.M.
,
Hof, J.R.
,
Stokroos, R.J.
,
Vanhoutte, E.K.
,
Admiraal, R.J.C.
,
Feenstra, I.
,
Kremer, H.
,
Kunst, H.P.M.
,
Pennings, R.J.E.
,
Yntema, H.G.
,
van Essen, A.J.
,
Free, R.H.
,
Klein-Wassink, J.S.
,
Admiraal, Ronald J.C.
,
Yntema, Helger G.
,
van Wijk, Erwin
,
del Castillo, Ignacio
,
Serra, Pau
,
Varela-Nieto, Isabel
,
Pennings, Ronald J.E.
,
Kremer, Hannie
Published in
American journal of human genetics
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Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction
by
Wesdorp, Mieke
,
de Koning Gans, Pia A. M.
,
Schraders, Margit
,
Oostrik, Jaap
,
Huynen, Martijn A.
,
Venselaar, Hanka
,
Beynon, Andy J.
,
van Gaalen, Judith
,
Piai, Vitória
,
Voermans, Nicol
,
van Rossum, Michelle M.
,
Hartel, Bas P.
,
Lelieveld, Stefan H.
,
Wiel, Laurens
,
Verbist, Berit
,
Rotteveel, Liselotte J.
,
van Dooren, Marieke F.
,
Lichtner, Peter
,
Kunst, Henricus P. M.
,
Feenstra, Ilse
,
Admiraal, Ronald J. C.
,
Yntema, Helger G.
,
Hoefsloot, Lies H.
,
Pennings, Ronald J. E.
,
Kremer, Hannie
Published in
Human genetics
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American Journal Of Human Genetics
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Hearing Research
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Human Genetics
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Journal Of Shoulder And Elbow Surgery
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Molecular Therapy. Nucleic Acids
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The American Journal Of Human Genetics
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Life Sciences & Biomedicine
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Science & Technology
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Female
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Humans
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Deafness
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Genetics & Heredity
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Antisense Oligonucleotides
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Arthroplasty, Replacement, Shoulder - Methods
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Audiology & Speech-Language Pathology
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Audiometry
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Audiometry, Pure-Tone
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Auditory Threshold
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