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6. Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome: one clinical entity? Mégarbané A; Al-Ali R; Choucair N; Lek M; Wang E; Ladjimi M; Rose CM; Hobeika R; Macary Y; Temanni R; Jithesh PV; Chouchane A; Sastry KS; Thomas R; Tomei S; Liu W; Marincola FM; MacArthur D; Chouchane L BMC Med Genet; 2016 Jun; 17(1):42. PubMed ID: 27282200 [TBL] [Abstract][Full Text] [Related]
7. West syndrome in a patient with Schinzel-Giedion syndrome. Miyake F; Kuroda Y; Naruto T; Ohashi I; Takano K; Kurosawa K J Child Neurol; 2015 Jun; 30(7):932-6. PubMed ID: 25028416 [TBL] [Abstract][Full Text] [Related]
8. Two cases of Temple-Baraitser syndrome: natural history and further delineation of the clinical and radiologic phenotypes. Shen JJ Clin Dysmorphol; 2015 Apr; 24(2):55-60. PubMed ID: 25629734 [TBL] [Abstract][Full Text] [Related]
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10. 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]
11. Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes. Lacombe D; Bioulac-Sage P; Sibout M; Daussac E; Lesure F; Manchart JP; Battin J Genet Couns; 1994; 5(3):251-6. PubMed ID: 7811425 [TBL] [Abstract][Full Text] [Related]
12. Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome. Chacon-Camacho OF; Vázquez J; Zenteno JC Am J Med Genet A; 2011 Jul; 155A(7):1716-20. PubMed ID: 21626675 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features. Carvalho E; Honjo R; Magalhães M; Yamamoto G; Rocha K; Naslavsky M; Zatz M; Passos-Bueno MR; Kim C; Bertola D Am J Med Genet A; 2015 May; 167A(5):1039-46. PubMed ID: 25663181 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis. Napoli G; Panzironi N; Traversa A; Catalanotto C; Pace V; Petrizzelli F; Giovannetti A; Lazzari S; Cogoni C; Tartaglia M; Carella M; Mazza T; Pizzuti A; Parisi C; Caputo V Mol Neurobiol; 2022 Aug; 59(8):4825-4838. PubMed ID: 35639255 [TBL] [Abstract][Full Text] [Related]
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18. 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]
19. Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies. Acuna-Hidalgo R; Deriziotis P; Steehouwer M; Gilissen C; Graham SA; van Dam S; Hoover-Fong J; Telegrafi AB; Destree A; Smigiel R; Lambie LA; Kayserili H; Altunoglu U; Lapi E; Uzielli ML; Aracena M; Nur BG; Mihci E; Moreira LM; Borges Ferreira V; Horovitz DD; da Rocha KM; Jezela-Stanek A; Brooks AS; Reutter H; Cohen JS; Fatemi A; Smitka M; Grebe TA; Di Donato N; Deshpande C; Vandersteen A; Marques Lourenço C; Dufke A; Rossier E; Andre G; Baumer A; Spencer C; McGaughran J; Franke L; Veltman JA; De Vries BB; Schinzel A; Fisher SE; Hoischen A; van Bon BW PLoS Genet; 2017 Mar; 13(3):e1006683. PubMed ID: 28346496 [TBL] [Abstract][Full Text] [Related]
20. Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant. Schwarz M; Ryba L; Křepelová A; Moslerová V; Zelinová M; Turnovec M; Martinková J; Kratochvílová L; Drahanský M; Macek M; Havlovicová M Am J Med Genet A; 2022 Apr; 188(4):1083-1087. PubMed ID: 34907639 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]