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Page 1
Causes of death in children with congenital anomalies up to age 10 in eight European countries.
Rissmann A, Tan J, Glinianaia SV, Rankin J, Pierini A, Santoro M, Coi A, Garne E, Loane M, Given J, Reid A, Aizpurua A, Akhmedzhanova D, Ballardini E, Barisic I, Cavero-Carbonell C, de Walle HEK, Gatt M, Gissler M, Heino A, Jordan S, Urhoj SK, Klungsøyr K, Lutke R, Mokoroa O, Neville AJ, Thayer DS, Wellesley DG, Yevtushok L, Zurriaga O, Morris J. Rissmann A, et al. Among authors: wellesley dg. BMJ Paediatr Open. 2023 Jun;7(1):e001617. doi: 10.1136/bmjpo-2022-001617. BMJ Paediatr Open. 2023. PMID: 37353235 Free PMC article.
The contribution of X-linked coding variation to severe developmental disorders.
Martin HC, Gardner EJ, Samocha KE, Kaplanis J, Akawi N, Sifrim A, Eberhardt RY, Tavares ALT, Neville MDC, Niemi MEK, Gallone G, McRae J; Deciphering Developmental Disorders Study; Wright CF, FitzPatrick DR, Firth HV, Hurles ME. Martin HC, et al. Nat Commun. 2021 Jan 27;12(1):627. doi: 10.1038/s41467-020-20852-3. Nat Commun. 2021. PMID: 33504798 Free PMC article.
The fetal valproate syndrome.
Wellesley D. Wellesley D. Am J Med Genet. 1988 Oct;31(2):475, 477-8. doi: 10.1002/ajmg.1320310231. Am J Med Genet. 1988. PMID: 3148280 No abstract available.
Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans.
Bouasker S, Patel N, Greenlees R, Wellesley D, Fares Taie L, Almontashiri NA, Baptista J, Alghamdi MA, Boissel S, Martinovic J, Prokudin I, Holden S, Mudhar HS, Riley LG, Nassif C, Attie-Bitach T, Miguet M, Delous M, Ernest S, Plaisancié J, Calvas P, Rozet JM, Khan AO, Hamdan FF, Jamieson RV, Alkuraya FS, Michaud JL, Chassaing N. Bouasker S, et al. J Med Genet. 2023 Mar;60(3):294-300. doi: 10.1136/jmedgenet-2022-108475. Epub 2022 Jul 5. J Med Genet. 2023. PMID: 35790350
The CHARGE syndrome.
Wellesley D. Wellesley D. Clin Genet. 1986 Nov;30(5):448. doi: 10.1111/j.1399-0004.1986.tb01908.x. Clin Genet. 1986. PMID: 3802565 No abstract available.
Autism, language and communication in children with sex chromosome trisomies.
Bishop DV, Jacobs PA, Lachlan K, Wellesley D, Barnicoat A, Boyd PA, Fryer A, Middlemiss P, Smithson S, Metcalfe K, Shears D, Leggett V, Nation K, Scerif G. Bishop DV, et al. Arch Dis Child. 2011 Oct;96(10):954-9. doi: 10.1136/adc.2009.179747. Epub 2010 Jul 23. Arch Dis Child. 2011. PMID: 20656736 Free PMC article.
125 results