Hypoglycaemia represents a clinically significant manifestation of PIK3CA‐ and CCND2‐associated segmental overgrowth von McDermott, J.H., Hickson, N., Banerjee, I., Murray, P.G., Ram, D., Metcalfe, K., Clayton‐Smith, J., Douzgou, S.

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AUTISM SPECTRUM DISORDERS FOLLOWING IN UTERO EXPOSURE TO ANTIEPILEPTIC DRUGS von BROMLEY, R. L, MAWER, G, CLAYTON-SMITH, J, BAKER, G. A

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Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual development von Thuresson, A‐C., Van Buggenhout, G., Sheth, F., Kamate, M., Andrieux, J., Clayton Smith, J., Soussi Zander, C.

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Assisted reproductive therapies and imprinting disorders—a preliminary British survey von Sutcliffe, A.G., Peters, C.J., Bowdin, S., Temple, K., Reardon, W., Wilson, L., Clayton-Smith, J., Brueton, L.A., Bannister, W., Maher, E.R.

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Selection and application of natural antimicrobials to control Clostridium perfringens in sous-vide chicken breasts inhibition of C. perfringens in sous-vide chicken von Smith, Clayton J, Olszewska, Magdalena A, Diez-Gonzalez, Francisco

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Dysmorphic features: an important clue to the diagnosis and severity of fetal anticonvulsant syndromes von Kini, U, Adab, N, Vinten, J, Fryer, A, Clayton-Smith, J

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Reconstruction techniques and clinical results of patellar tendon ruptures: Evidence today von Gilmore, Jack H, Clayton-Smith, Zoë J, Aguilar, Marc, Pneumaticos, Spiros G, Giannoudis, Peter V

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Angelman syndrome: a review of the clinical and genetic aspects von Clayton-Smith, J, Laan, L

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The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome von Schönewolf-Greulich, B., Tejada, M.-I., Stephens, K., Hadzsiev, K., Gauthier, J., Brøndum-Nielsen, K., Pfundt, R., Ravn, K., Maortua, H., Gener, B., Martínez-Bouzas, C., Piton, A., Rouleau, G., Clayton-Smith, J., Kleefstra, T., Bisgaard, A.-M., Tümer, Z.

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Cerebral screening in patients with hereditary haemorrhagic telangiectasia von Jackson, A., Briggs, T. A., Clayton-Smith, J.

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Dysmorphology services: a snapshot of current practices and a vision for the future von Douzgou, S., Chervinsky, E., Gyftodimou, Y., Kitsiou-Tzeli, S., Shalev, S., Kanavakis, E., Donnai, D., Clayton-Smith, J.

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Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome von Balikova, I, Lehesjoki, A.E, de Ravel, T.J.L, Thienpont, B, Chandler, K.E, Clayton-Smith, J, Träskelin, A.L, Fryns, J.P, Vermeesch, J.R

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Further delineation of Pitt–Hopkins syndrome: phenotypic and genotypic description of 16 novel patients von Zweier, C, Sticht, H, Bijlsma, E K, Clayton-Smith, J, Boonen, S E, Fryer, A, Greally, M T, Hoffmann, L, den Hollander, N S, Jongmans, M, Kant, S G, King, M D, Lynch, S A, McKee, S, Midro, A T, Park, S-M, Ricotti, V, Tarantino, E, Wessels, M, Peippo, M, Rauch, A

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Low-dose in vivo protection and neutralization across SARS-CoV-2 variants by monoclonal antibody combinations von Dussupt, Vincent, Sankhala, Rajeshwer S., Mendez-Rivera, Letzibeth, Townsley, Samantha M., Schmidt, Fabian, Wieczorek, Lindsay, Lal, Kerri G., Donofrio, Gina C., Tran, Ursula, Jackson, Nathaniel D., Zaky, Weam I., Zemil, Michelle, Tritsch, Sarah R., Chen, Wei-Hung, Martinez, Elizabeth J., Ahmed, Aslaa, Choe, Misook, Chang, William C., Hajduczki, Agnes, Jian, Ningbo, Peterson, Caroline E., Rees, Phyllis A., Rutkowska, Magdalena, Slike, Bonnie M., Selverian, Christopher N., Swafford, Isabella, Teng, I-Ting, Thomas, Paul V., Zhou, Tongqing, Smith, Clayton J., Currier, Jeffrey R., Kwong, Peter D., Rolland, Morgane, Davidson, Edgar, Doranz, Benjamin J., Mores, Christopher N., Hatziioannou, Theodora, Reiley, William W., Bieniasz, Paul D., Paquin-Proulx, Dominic, Gromowski, Gregory D., Polonis, Victoria R., Michael, Nelson L., Modjarrad, Kayvon, Joyce, M. Gordon, Krebs, Shelly J.

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Aarskog-Scott syndrome: Clinical update and report of nine novel mutations of the FGD1 gene von Orrico, A., Galli, L., Faivre, L., Clayton-Smith, J., Azzarello-Burri, S.M., Hertz, J.M., Jacquemont, S., Taurisano, R., Arroyo Carrera, I., Tarantino, E., Devriendt, K., Melis, D., Thelle, T., Meinhardt, U., Sorrentino, V.

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Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males von Clayton-Smith, J, Watson, P, Ramsden, S, Black, GCM

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Systematic screening of FBN1 gene unclassified missense variants for splice abnormalities von Robinson, DO, Lin, F, Lyon, M, Raponi, M, Cross, E, White, HE, Cox, H, Clayton-Smith, J, Baralle, D

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Neurodevelopmental outcomes in children and adults with Fetal Valproate Spectrum Disorder: A contribution from the ConcePTION project von Bluett-Duncan, M., Astill, D., Charbak, R., Clayton-Smith, J., Cole, S., Cook, P.A., Cozens, J., Keely, K., Morris, J., Mukherjee, R., Murphy, E., Turnpenny, P., Williams, J., Wood, A.G., Yates, L.M., Bromley, R.L.

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The longer term outcome of children born to mothers with epilepsy von Adab, N, Kini, U, Vinten, J, Ayres, J, Baker, G, Clayton-Smith, J, Coyle, H, Fryer, A, Gorry, J, Gregg, J, Mawer, G, Nicolaides, P, Pickering, L, Tunnicliffe, L, Chadwick, D W

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A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome von Day, R, Beckett, B, Donnai, D, Fryer, A, Heidenblad, M, Howard, P, Kerr, B, Mansour, S, Maye, U, McKee, S, Mohammed, S, Sweeney, E, Tassabehji, M, De Vries, BBA, Clayton-Smith, J

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