These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
169 related articles for article (PubMed ID: 25712757)
1. MEIS2 involvement in cardiac development, cleft palate, and intellectual disability. Louw JJ; Corveleyn A; Jia Y; Hens G; Gewillig M; Devriendt K Am J Med Genet A; 2015 May; 167A(5):1142-6. PubMed ID: 25712757 [TBL] [Abstract][Full Text] [Related]
2. Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study. Gangfuß A; Yigit G; Altmüller J; Nürnberg P; Czeschik JC; Wollnik B; Bögershausen N; Burfeind P; Wieczorek D; Kaiser F; Roos A; Kölbel H; Schara-Schmidt U; Kuechler A Am J Med Genet A; 2021 Apr; 185(4):1216-1221. PubMed ID: 33427397 [TBL] [Abstract][Full Text] [Related]
3. De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features. Douglas G; Cho MT; Telegrafi A; Winter S; Carmichael J; Zackai EH; Deardorff MA; Harr M; Williams L; Psychogios A; Erwin AL; Grebe T; Retterer K; Juusola J Am J Med Genet A; 2018 Sep; 176(9):1845-1851. PubMed ID: 30055086 [TBL] [Abstract][Full Text] [Related]
4. Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability. Verheije R; Kupchik GS; Isidor B; Kroes HY; Lynch SA; Hawkes L; Hempel M; Gelb BD; Ghoumid J; D'Amours G; Chandler K; Dubourg C; Loddo S; Tümer Z; Shaw-Smith C; Nizon M; Shevell M; Van Hoof E; Anyane-Yeboa K; Cerbone G; Clayton-Smith J; Cogné B; Corre P; Corveleyn A; De Borre M; Hjortshøj TD; Fradin M; Gewillig M; Goldmuntz E; Hens G; Lemyre E; Journel H; Kini U; Kortüm F; Le Caignec C; Novelli A; Odent S; Petit F; Revah-Politi A; Stong N; Strom TM; van Binsbergen E; ; Devriendt K; Breckpot J Eur J Hum Genet; 2019 Feb; 27(2):278-290. PubMed ID: 30291340 [TBL] [Abstract][Full Text] [Related]
5. Haploinsufficiency of MEIS2 is associated with orofacial clefting and learning disability. Johansson S; Berland S; Gradek GA; Bongers E; de Leeuw N; Pfundt R; Fannemel M; Rødningen O; Brendehaug A; Haukanes BI; Hovland R; Helland G; Houge G Am J Med Genet A; 2014 Jul; 164A(7):1622-6. PubMed ID: 24678003 [TBL] [Abstract][Full Text] [Related]
6. MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotype. Giliberti A; Currò A; Papa FT; Frullanti E; Ariani F; Coriolani G; Grosso S; Renieri A; Mari F Eur J Med Genet; 2020 Jan; 63(1):103627. PubMed ID: 30735726 [TBL] [Abstract][Full Text] [Related]
7. De novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux. Fujita A; Isidor B; Piloquet H; Corre P; Okamoto N; Nakashima M; Tsurusaki Y; Saitsu H; Miyake N; Matsumoto N J Hum Genet; 2016 Sep; 61(9):835-8. PubMed ID: 27225850 [TBL] [Abstract][Full Text] [Related]
8. A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome. Santoro C; Riccio S; Palladino F; Aliberti F; Carotenuto M; Zanobio M; Peduto C; Nigro V; Perrotta S; Piluso G Eur J Med Genet; 2021 May; 64(5):104190. PubMed ID: 33722742 [TBL] [Abstract][Full Text] [Related]
9. MEIS2 sequence variant in a child with intellectual disability and cardiac defects: Expansion of the phenotypic spectrum and documentation of low-level mosaicism in an unaffected parent. Su JX; Velsher LS; Juusola J; Nezarati MM Am J Med Genet A; 2021 Jan; 185(1):300-303. PubMed ID: 33091211 [TBL] [Abstract][Full Text] [Related]
10. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing. Zarate YA; Perry H; Ben-Omran T; Sellars EA; Stein Q; Almureikhi M; Simmons K; Klein O; Fish J; Feingold M; Douglas J; Kruer MC; Si Y; Mao R; McKnight D; Gibellini F; Retterer K; Slavotinek A Am J Med Genet A; 2015 May; 167A(5):1026-32. PubMed ID: 25885067 [TBL] [Abstract][Full Text] [Related]
11. Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome. Cafiero C; Marangi G; Orteschi D; Ali M; Asaro A; Ponzi E; Moncada A; Ricciardi S; Murdolo M; Mancano G; Contaldo I; Leuzzi V; Battaglia D; Mercuri E; Slavotinek AM; Zollino M Eur J Hum Genet; 2015 Nov; 23(11):1499-504. PubMed ID: 25712080 [TBL] [Abstract][Full Text] [Related]
13. SATB2-associated syndrome presenting with Rett-like phenotypes. Lee JS; Yoo Y; Lim BC; Kim KJ; Choi M; Chae JH Clin Genet; 2016 Jun; 89(6):728-32. PubMed ID: 26596517 [TBL] [Abstract][Full Text] [Related]
14. Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septum. Crowley MA; Conlin LK; Zackai EH; Deardorff MA; Thiel BD; Spinner NB Am J Med Genet A; 2010 May; 152A(5):1326-7. PubMed ID: 20425846 [No Abstract] [Full Text] [Related]
15. Cleft Lip Palate in a Patient with 5q14.3 Deletion Syndrome: A Possible Unreported Feature? Fernández Hernández L; Alcántara Ortigoza MA; Ramos Angeles SE; González-Del Angel A Cytogenet Genome Res; 2021; 161(12):556-563. PubMed ID: 35021179 [TBL] [Abstract][Full Text] [Related]
16. Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation. Asadollahi R; Zweier M; Gogoll L; Schiffmann R; Sticht H; Steindl K; Rauch A Eur J Med Genet; 2017 Sep; 60(9):451-464. PubMed ID: 28645799 [TBL] [Abstract][Full Text] [Related]
17. Novel homozygous mutation, c.400C>T (p.Arg134*), in the PVRL1 gene underlies cleft lip/palate-ectodermal dysplasia syndrome in an Asian patient. Yoshida K; Hayashi R; Fujita H; Kubota M; Kondo M; Shimomura Y; Niizeki H J Dermatol; 2015 Jul; 42(7):715-9. PubMed ID: 25913853 [TBL] [Abstract][Full Text] [Related]
18. A ZFHX4 mutation associated with a recognizable neuropsychological and facial phenotype. Fontana P; Ginevrino M; Bejo K; Cantalupo G; Ciavarella M; Lombardi C; Maioli M; Scarano F; Costabile C; Novelli A; Lonardo F Eur J Med Genet; 2021 Nov; 64(11):104321. PubMed ID: 34461323 [TBL] [Abstract][Full Text] [Related]
19. Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome. Prontera P; Garelli E; Isidori I; Mencarelli A; Carando A; Silengo MC; Donti E Am J Med Genet A; 2011 Nov; 155A(11):2746-9. PubMed ID: 21990121 [TBL] [Abstract][Full Text] [Related]
20. Cardiofacioneurodevelopmental syndrome: Report of a novel patient and expansion of the phenotype. Abdalla E; Alawi M; Meinecke P; Kutsche K; Harms FL Am J Med Genet A; 2022 Aug; 188(8):2448-2453. PubMed ID: 35451546 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]