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.
147 related articles for article (PubMed ID: 22838235)
21. Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G > A (p.R357Q) variant. Chen D; Su J; Huang X; Chen H; Jiang T; Zhi C; Zhou Z; Zhang B; Yu L; Jiang X Hum Cell; 2024 May; 37(3):832-839. PubMed ID: 38372889 [TBL] [Abstract][Full Text] [Related]
22. Laband syndrome: a case report. Bazopoulou-Kyrkanidou E; Papagianoulis L; Papanicolaou S; Mavrou A J Oral Pathol Med; 1990 Sep; 19(8):385-7. PubMed ID: 2250229 [TBL] [Abstract][Full Text] [Related]
23. Unusual neuroradiological features in Schinzel-Giedion syndrome: a novel case. Lestner JM; Chong WK; Offiiah A; Kefas J; Vandersteen AM Clin Dysmorphol; 2012 Jul; 21(3):152-154. PubMed ID: 22473152 [No Abstract] [Full Text] [Related]
24. Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations. Chadwick B; Hunter B; Hunter L; Aldred M; Wilkie A Oral Surg Oral Med Oral Pathol; 1994 Jul; 78(1):57-63. PubMed ID: 8078665 [TBL] [Abstract][Full Text] [Related]
25. Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome. Kortüm F; Caputo V; Bauer CK; Stella L; Ciolfi A; Alawi M; Bocchinfuso G; Flex E; Paolacci S; Dentici ML; Grammatico P; Korenke GC; Leuzzi V; Mowat D; Nair LD; Nguyen TT; Thierry P; White SM; Dallapiccola B; Pizzuti A; Campeau PM; Tartaglia M; Kutsche K Nat Genet; 2015 Jun; 47(6):661-7. PubMed ID: 25915598 [TBL] [Abstract][Full Text] [Related]
26. Epilepsy in KCNH1-related syndromes. Mastrangelo M; Scheffer IE; Bramswig NC; Nair LD; Myers CT; Dentici ML; Korenke GC; Schoch K; Campeau PM; White SM; Shashi V; Kansagra S; Van Essen AJ; Leuzzi V Epileptic Disord; 2016 Jun; 18(2):123-36. PubMed ID: 27267311 [TBL] [Abstract][Full Text] [Related]
27. Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca Bauer CK; Schneeberger PE; Kortüm F; Altmüller J; Santos-Simarro F; Baker L; Keller-Ramey J; White SM; Campeau PM; Gripp KW; Kutsche K Am J Hum Genet; 2019 Jun; 104(6):1139-1157. PubMed ID: 31155282 [TBL] [Abstract][Full Text] [Related]
29. Zimmermann-Laband syndrome in a patient with severe mental retardation. Van Buggenhout GJ; Brunner HG; Trommelen JC; Hamel BC Genet Couns; 1995; 6(4):321-7. PubMed ID: 8775419 [TBL] [Abstract][Full Text] [Related]
30. A new case of Zimmermann-Laband syndrome with atypical retinitis pigmentosa. Koch P; Wettstein A; Knauber J; Zaun H Acta Derm Venereol; 1992 Sep; 72(5):376-9. PubMed ID: 1361289 [TBL] [Abstract][Full Text] [Related]
31. Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes. Gao X; Dai P; Yuan YY Hum Genet; 2022 Apr; 141(3-4):821-838. PubMed ID: 34232384 [TBL] [Abstract][Full Text] [Related]
32. Treatment of gingival fibromatosis associated with Zimmermann-Laband syndrome. Holzhausen M; Ribeiro FS; Gonçalves D; Corrêa FO; Spolidorio LC; Orrico SR J Periodontol; 2005 Sep; 76(9):1559-62. PubMed ID: 16171447 [TBL] [Abstract][Full Text] [Related]
33. Patients with Aubert Mucca M; Patat O; Whalen S; Arnaud L; Barcia G; Buratti J; Cogné B; Doummar D; Karsenty C; Kenis S; Leguern E; Lesca G; Nava C; Nizon M; Piton A; Valence S; Villard L; Weckhuysen S; Keren B; Mignot C J Med Genet; 2022 May; 59(5):505-510. PubMed ID: 33811134 [TBL] [Abstract][Full Text] [Related]
34. Syndromes with gingival fibromatosis: A systematic review. Costa CRR; Braz SV; de Toledo IP; Martelli-Júnior H; Mazzeu JF; Guerra ENS; Coletta RD; Acevedo AC Oral Dis; 2021 May; 27(4):881-893. PubMed ID: 32335995 [TBL] [Abstract][Full Text] [Related]
35. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K Gripp KW; Smithson SF; Scurr IJ; Baptista J; Majumdar A; Pierre G; Williams M; Henderson LB; Wentzensen IM; McLaughlin H; Leeuwen L; Simon MEH; van Binsbergen E; Dinulos MBP; Kaplan JD; McRae A; Superti-Furga A; Good JM; Kutsche K Eur J Hum Genet; 2021 Sep; 29(9):1384-1395. PubMed ID: 33594261 [TBL] [Abstract][Full Text] [Related]
36. Zimmermann-Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions. Stefanova M; Atanassov D; Krastev T; Fuchs S; Kutsche K Am J Med Genet A; 2003 Mar; 117A(3):289-94. PubMed ID: 12599195 [TBL] [Abstract][Full Text] [Related]
38. "Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes. Hamilton MJ; Suri M Adv Genet; 2020; 105():137-174. PubMed ID: 32560786 [TBL] [Abstract][Full Text] [Related]
39. Progressive brain atrophy in Schinzel-Giedion syndrome with a SETBP1 mutation. Takeuchi A; Okamoto N; Fujinaga S; Morita H; Shimizu J; Akiyama T; Ninomiya S; Takanashi J; Kubo T Eur J Med Genet; 2015 Aug; 58(8):369-71. PubMed ID: 26096993 [TBL] [Abstract][Full Text] [Related]
40. Zimmermann-Laband syndrome in an infant with an atypical histologic finding. Atabek ME; Pirgon O; Sert A; Toy H Pediatr Dev Pathol; 2005; 8(6):654-7. PubMed ID: 16267629 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]