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Correction: Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.
Genet Med. 2021 Jul;23(7):1376-1377. doi: 10.1038/s41436-021-01202-0.
Genet Med. 2021.
PMID: 34040196
Free PMC article.
No abstract available.
Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypes.
Martin-Almedina S, Ogmen K, Sackey E, Grigoriadis D, Karapouliou C, Nadarajah N, Ebbing C, Lord J, Mellis R, Kortuem F, Dinulos MB, Polun C, Bale S, Atton G, Robinson A, Reigstad H, Houge G, von der Wense A, Becker WH, Jeffery S, Mortimer PS, Gordon K, Josephs KS, Robart S, Kilby MD, Vallee S, Gorski JL, Hempel M, Berland S, Mansour S, Ostergaard P.
Martin-Almedina S, et al. Among authors: atton g.
Genet Med. 2021 Jul;23(7):1315-1324. doi: 10.1038/s41436-021-01136-7. Epub 2021 Apr 16.
Genet Med. 2021.
PMID: 33864021
Free PMC article.
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The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review.
Atton G, Gordon K, Brice G, Keeley V, Riches K, Ostergaard P, Mortimer P, Mansour S.
Atton G, et al.
Eur J Hum Genet. 2015 Dec;23(12):1634-9. doi: 10.1038/ejhg.2015.41. Epub 2015 Mar 25.
Eur J Hum Genet. 2015.
PMID: 25804399
Free PMC article.
Review.
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Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Fotiou E, Martin-Almedina S, Simpson MA, Lin S, Gordon K, Brice G, Atton G, Jeffery I, Rees DC, Mignot C, Vogt J, Homfray T, Snyder MP, Rockson SG, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.
Fotiou E, et al. Among authors: atton g.
Nat Commun. 2019 Apr 26;10(1):1951. doi: 10.1038/s41467-019-09905-4.
Nat Commun. 2019.
PMID: 31028252
Free PMC article.
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Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.
Fotiou E, Martin-Almedina S, Simpson MA, Lin S, Gordon K, Brice G, Atton G, Jeffery I, Rees DC, Mignot C, Vogt J, Homfray T, Snyder MP, Rockson SG, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.
Fotiou E, et al. Among authors: atton g.
Nat Commun. 2015 Sep 3;6:8085. doi: 10.1038/ncomms9085.
Nat Commun. 2015.
PMID: 26333996
Free PMC article.
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EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.
Martin-Almedina S, Martinez-Corral I, Holdhus R, Vicente A, Fotiou E, Lin S, Petersen K, Simpson MA, Hoischen A, Gilissen C, Jeffery H, Atton G, Karapouliou C, Brice G, Gordon K, Wiseman JW, Wedin M, Rockson SG, Jeffery S, Mortimer PS, Snyder MP, Berland S, Mansour S, Makinen T, Ostergaard P.
Martin-Almedina S, et al. Among authors: atton g.
J Clin Invest. 2016 Aug 1;126(8):3080-8. doi: 10.1172/JCI85794. Epub 2016 Jul 11.
J Clin Invest. 2016.
PMID: 27400125
Free PMC article.
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Epidemiology of Robin sequence: geographical variation in the UK/Ireland.
Atton G, Baralle D.
Atton G, et al.
Arch Dis Child. 2024 Feb 19;109(3):177-178. doi: 10.1136/archdischild-2023-326079.
Arch Dis Child. 2024.
PMID: 38199816
No abstract available.
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Extending the phenotypes associated with TRIO gene variants in a cohort of 25 patients and review of the literature.
Gazdagh G, Hunt D, Gonzalez AMC, Rodriguez MP, Chaudhry A, Madruga M, Vansenne F, Shears D, Curie A, Stattin EL, Anderlid BM, Trajkova S, Angelovska ES, McWilliam C, Wyatt PR, O'Driscoll M, Atton G, Bergman AK, Zacher P, Mewasingh LD, López AG, Alonso-Luengo O, Wai HA, Rohde O, Boiroux P, Debant A, Schmidt S, Baralle D.
Gazdagh G, et al. Among authors: atton g.
Am J Med Genet A. 2023 Jul;191(7):1722-1740. doi: 10.1002/ajmg.a.63194. Epub 2023 Mar 29.
Am J Med Genet A. 2023.
PMID: 36987741
Review.
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