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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Am J Hum Genet. 2021 Jun 3;108(6):1138-1150. doi: 10.1016/j.ajhg.2021.04.007. Epub 2021 Apr 27.
Am J Hum Genet. 2021.
PMID: 33909992
Free PMC article.
ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.
Kushary ST, Revah-Politi A, Barua S, Ganapathi M, Accogli A, Aggarwal V, Brunetti-Pierri N, Cappuccio G, Capra V, Fagerberg CR, Gazdagh G, Guzman E, Hadonou M, Harrison V, Havelund K, Iancu D, Kraus A, Lippa NC, Mansukhani M, McBrian D, McEntagart M, Pacio-Míguez M, Palomares-Bralo M, Pottinger C, Ruivenkamp CAL, Sacco O, Santen GWE, Santos-Simarro F, Scala M, Short J, Sørensen KP, Woods CG; DDD Study; TUDP Consortium; Anyane Yeboa K.
Kushary ST, et al. Among authors: hadonou m.
Am J Med Genet A. 2021 Dec;185(12):3740-3753. doi: 10.1002/ajmg.a.62445. Epub 2021 Jul 31.
Am J Med Genet A. 2021.
PMID: 34331327
Free PMC article.
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Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation.
Ocansey S, Pullen D, Atkinson P, Clarke A, Hadonou M, Crosby C, Short J, Lloyd IC, Smedley D, Assunta A, Shah P, McEntagart M; Genomics England Research Consortium.
Ocansey S, et al. Among authors: hadonou m.
Clin Dysmorphol. 2022 Jan 1;31(1):11-17. doi: 10.1097/MCD.0000000000000397.
Clin Dysmorphol. 2022.
PMID: 34654017
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The effect of soccer training on the levels of atherosclerotic lipids in the blood of obese subjects.
Dansou P, Tolly PL, Yèhouénou B, Tossou R, Hadonou ML.
Dansou P, et al. Among authors: hadonou ml.
Sante. 2000 Nov-Dec;10(6):393-7.
Sante. 2000.
PMID: 11226935
Free article.
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