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.
197 related articles for article (PubMed ID: 22522176)
21. Clinical and molecular genetic characterization of familial MECP2 duplication syndrome in a Chinese family. Li X; Xie H; Chen Q; Yu X; Yi Z; Li E; Zhang T; Wang J; Zhong J; Chen X BMC Med Genet; 2017 Nov; 18(1):131. PubMed ID: 29141583 [TBL] [Abstract][Full Text] [Related]
22. Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genes. Sinibaldi L; Parisi V; Lanciotti S; Fontana P; Kuechler A; Baujat G; Torres B; Koetting J; Splendiani A; Postorivo D; Beygo J; Garaci FG; Malan V; Lüdecke HJ; Guida V; Krumbiegel M; Lonardo F; Novelli A; Albrecht B; Perria C; Scarano G; Spielmann M; Nardone AM; Battaglia A; Brancati F; Bernardini L Clin Genet; 2019 Sep; 96(3):246-253. PubMed ID: 31090057 [TBL] [Abstract][Full Text] [Related]
23. A sibship with duplication of Xq28 inherited from the mother; genomic characterization and clinical outcomes. Yon DK; Park JE; Kim SJ; Shim SH; Chae KY BMC Med Genet; 2017 Mar; 18(1):30. PubMed ID: 28302064 [TBL] [Abstract][Full Text] [Related]
24. MECP2 duplication syndrome in a patient from Cameroon. Tekendo-Ngongang C; Dahoun S; Nguefack S; Moix I; Gimelli S; Zambo H; Morris MA; Sloan-Béna F; Wonkam A Am J Med Genet A; 2020 Apr; 182(4):619-622. PubMed ID: 32052928 [TBL] [Abstract][Full Text] [Related]
25. De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation. Fieremans N; Bauters M; Belet S; Verbeeck J; Jansen AC; Seneca S; Roelens F; De Baere E; Marynen P; Froyen G Hum Genet; 2014 Nov; 133(11):1359-67. PubMed ID: 25037250 [TBL] [Abstract][Full Text] [Related]
26. Progressive cerebellar degenerative changes in the severe mental retardation syndrome caused by duplication of MECP2 and adjacent loci on Xq28. Reardon W; Donoghue V; Murphy AM; King MD; Mayne PD; Horn N; Birk Møller L Eur J Pediatr; 2010 Aug; 169(8):941-9. PubMed ID: 20177701 [TBL] [Abstract][Full Text] [Related]
27. Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability. Andersen EF; Baldwin EE; Ellingwood S; Smith R; Lamb AN Am J Med Genet A; 2014 Jul; 164A(7):1795-801. PubMed ID: 24700761 [TBL] [Abstract][Full Text] [Related]
28. Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions. El-Hattab AW; Fang P; Jin W; Hughes JR; Gibson JB; Patel GS; Grange DK; Manwaring LP; Patel A; Stankiewicz P; Cheung SW J Med Genet; 2011 Dec; 48(12):840-50. PubMed ID: 21984752 [TBL] [Abstract][Full Text] [Related]
29. Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections. Smyk M; Obersztyn E; Nowakowska B; Nawara M; Cheung SW; Mazurczak T; Stankiewicz P; Bocian E Am J Med Genet B Neuropsychiatr Genet; 2008 Sep; 147B(6):799-806. PubMed ID: 18165974 [TBL] [Abstract][Full Text] [Related]
30. Further delineation of the Miguet M; Faivre L; Amiel J; Nizon M; Touraine R; Prieur F; Pasquier L; Lefebvre M; Thevenon J; Dubourg C; Julia S; Sarret C; Remerand G; Francannet C; Laffargue F; Boespflug-Tanguy O; David A; Isidor B; Vigneron J; Leheup B; Lambert L; Philippe C; Béri-Dexheimer M; Cuisset JM; Andrieux J; Plessis G; Toutain A; Guibaud L; Cormier-Daire V; Rio M; Bonnefont JP; Echenne B; Journel H; Burglen L; Chantot-Bastaraud S; Bienvenu T; Baumann C; Perrin L; Drunat S; Jouk PS; Dieterich K; Devillard F; Lacombe D; Philip N; Sigaudy S; Moncla A; Missirian C; Badens C; Perreton N; Thauvin-Robinet C; AChro-Puce R; Pedespan JM; Rooryck C; Goizet C; Vincent-Delorme C; Duban-Bedu B; Bahi-Buisson N; Afenjar A; Maincent K; Héron D; Alessandri JL; Martin-Coignard D; Lesca G; Rossi M; Raynaud M; Callier P; Mosca-Boidron AL; Marle N; Coutton C; Satre V; Caignec CL; Malan V; Romana S; Keren B; Tabet AC; Kremer V; Scheidecker S; Vigouroux A; Lackmy-Port-Lis M; Sanlaville D; Till M; Carneiro M; Gilbert-Dussardier B; Willems M; Van Esch H; Portes VD; El Chehadeh S J Med Genet; 2018 Jun; 55(6):359-371. PubMed ID: 29618507 [TBL] [Abstract][Full Text] [Related]
31. Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review. El-Hattab AW; Schaaf CP; Fang P; Roeder E; Kimonis VE; Church JA; Patel A; Cheung SW BMC Med Genet; 2015 Mar; 16():12. PubMed ID: 25927380 [TBL] [Abstract][Full Text] [Related]
32. X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome. Møller RS; Jensen LR; Maas SM; Filmus J; Capurro M; Hansen C; Marcelis CL; Ravn K; Andrieux J; Mathieu M; Kirchhoff M; Rødningen OK; de Leeuw N; Yntema HG; Froyen G; Vandewalle J; Ballon K; Klopocki E; Joss S; Tolmie J; Knegt AC; Lund AM; Hjalgrim H; Kuss AW; Tommerup N; Ullmann R; de Brouwer AP; Strømme P; Kjaergaard S; Tümer Z; Kleefstra T Hum Genet; 2014 May; 133(5):625-38. PubMed ID: 24326587 [TBL] [Abstract][Full Text] [Related]
33. De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardation. Velinov M; Novelli A; Gu H; Fenko M; Dolzhanskaya N; Bernardini L; Capalbo A; Dallapiccola B; Jenkins EC; Brown WT Clin Dysmorphol; 2009 Jan; 18(1):9-12. PubMed ID: 19090026 [TBL] [Abstract][Full Text] [Related]
34. MECP2 duplication: possible cause of severe phenotype in females. Scott Schwoerer J; Laffin J; Haun J; Raca G; Friez MJ; Giampietro PF Am J Med Genet A; 2014 Apr; 164A(4):1029-34. PubMed ID: 24458799 [TBL] [Abstract][Full Text] [Related]
35. Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. Ramocki MB; Peters SU; Tavyev YJ; Zhang F; Carvalho CM; Schaaf CP; Richman R; Fang P; Glaze DG; Lupski JR; Zoghbi HY Ann Neurol; 2009 Dec; 66(6):771-82. PubMed ID: 20035514 [TBL] [Abstract][Full Text] [Related]
36. Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance. Clayton-Smith J; Walters S; Hobson E; Burkitt-Wright E; Smith R; Toutain A; Amiel J; Lyonnet S; Mansour S; Fitzpatrick D; Ciccone R; Ricca I; Zuffardi O; Donnai D Eur J Hum Genet; 2009 Apr; 17(4):434-43. PubMed ID: 18854860 [TBL] [Abstract][Full Text] [Related]
37. Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2. Fukushi D; Yamada K; Nomura N; Naiki M; Kimura R; Yamada Y; Kumagai T; Yamaguchi K; Miyake Y; Wakamatsu N Am J Med Genet A; 2014 Apr; 164A(4):924-33. PubMed ID: 24478188 [TBL] [Abstract][Full Text] [Related]
38. [Diagnosis of MECP2 duplication syndrome with molecular genetic techniques]. Yi Z; Wang S; Li L; Wu H; Ma Y; Qi Y; Pan H Zhonghua Er Ke Za Zhi; 2014 Dec; 52(12):937-41. PubMed ID: 25619353 [TBL] [Abstract][Full Text] [Related]
39. Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation. Honda S; Satomura S; Hayashi S; Imoto I; Nakagawa E; Goto Y; Inazawa J; J Hum Genet; 2012 Jan; 57(1):73-7. PubMed ID: 22129561 [TBL] [Abstract][Full Text] [Related]
40. De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features. Neira VA; Romero-Espinoza P; Rojas-Martínez A; Ortiz-López R; Córdova-Fletes C; Plaja A; Barros-Núñez P Gene; 2013 Jul; 524(2):381-5. PubMed ID: 23639959 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]