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Morison, LD, Kennis, MGP, Rots, D, Bouman, A, Kummeling, J, Palmer, E, Vogel, AP, Liegeois, F, Brignell, A, Srivastava, S, et al.
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals..
J Med Genet
61(6)
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578 -585
2024
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Engelen, MM, Franken, M-CJP, Stipdonk, LW, Horton, SE, Jackson, VE, Reilly, S, Morgan, AT, Fisher, SE, van Dulmen, S, Eising, E.
The Association Between Stuttering Burden and Psychosocial Aspects of Life in Adults..
J Speech Lang Hear Res
67(5)
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1385 -1399
2024
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Wu, S-T, Feng, Y, Song, R, Qi, Y, Li, L, Lu, D, Wang, Y, Wu, W, Morgan, A, Wang, X, et al.
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation..
J Am Soc Nephrol
35(5)
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533 -548
2024
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Kleinendorst, L, Abawi, O, Vos, N, van der Valk, ES, Maas, SM, Morgan, AT, Hildebrand, MS, Da Silva, JD, Florijn, RJ, Lauffer, P, et al.
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity..
Clin Obes
e12661
2024
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Meng, Y, Best, S, Amor, DJ, Braden, R, Morgan, AT, Goranitis, I.
The value of genomic testing in severe childhood speech disorders..
Eur J Hum Genet
32(4)
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440 -447
2024
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