149 related articles for article (PubMed ID: 25434475)
21. Ritscher-Schinzel or 3C syndrome, with heterochromatic iris.
Hatzidaki E; Manoura A; Korakaki E; Germanakis J; Karabekios S; Giannakopoulou C
Pediatr Int; 2003 Oct; 45(5):574-6. PubMed ID: 14521535
[No Abstract] [Full Text] [Related]
22. Increased nuchal translucency thickness: a potential indicator for Ritscher-Schinzel syndrome.
Rusnak AJ; Hadfield MI; Chudley AE; Marles SL; Reid GJ; Chodirker BN
Fetal Diagn Ther; 2008; 24(4):395-9. PubMed ID: 18957854
[TBL] [Abstract][Full Text] [Related]
23. The 3C syndrome: evolution of the phenotype and growth hormone deficiency.
Wheeler PG; Sadeghi-Nejad A; Elias ER
Am J Med Genet; 1999 Nov; 87(1):61-4. PubMed ID: 10528249
[TBL] [Abstract][Full Text] [Related]
24. Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome.
Kolanczyk M; Krawitz P; Hecht J; Hupalowska A; Miaczynska M; Marschner K; Schlack C; Emmerich D; Kobus K; Kornak U; Robinson PN; Plecko B; Grangl G; Uhrig S; Mundlos S; Horn D
Eur J Hum Genet; 2015 May; 23(5):720. PubMed ID: 25880334
[No Abstract] [Full Text] [Related]
25. Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.
Marles SL; Chodirker BN; Greenberg CR; Chudley AE
Am J Med Genet; 1995 May; 56(4):343-50. PubMed ID: 7604842
[TBL] [Abstract][Full Text] [Related]
26. A novel mutation in KIAA0196: identification of a gene involved in Ritscher-Schinzel/3C syndrome in a First Nations cohort.
Elliott AM; Simard LR; Coghlan G; Chudley AE; Chodirker BN; Greenberg CR; Burch T; Ly V; Hatch GM; Zelinski T
J Med Genet; 2013 Dec; 50(12):819-22. PubMed ID: 24065355
[TBL] [Abstract][Full Text] [Related]
27. Cerebellar hypoplasia in a patient with velo-cardio-facial syndrome.
Devriendt K; Thienen MN; Swillen A; Fryns JP
Dev Med Child Neurol; 1996 Oct; 38(10):949-53. PubMed ID: 8870617
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis.
Albano LM; Sakae PP; Mataloun MM; Leone CR; Bertola DR; Kim CA
Rev Hosp Clin Fac Med Sao Paulo; 2004 Apr; 59(2):89-92. PubMed ID: 15122424
[TBL] [Abstract][Full Text] [Related]
30. Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndrome.
Healy MD; McNally KE; Butkovič R; Chilton M; Kato K; Sacharz J; McConville C; Moody ERR; Shaw S; Planelles-Herrero VJ; Yadav SKN; Ross J; Borucu U; Palmer CS; Chen KE; Croll TI; Hall RJ; Caruana NJ; Ghai R; Nguyen THD; Heesom KJ; Saitoh S; Berger I; Schaffitzel C; Williams TA; Stroud DA; Derivery E; Collins BM; Cullen PJ
Cell; 2023 May; 186(10):2219-2237.e29. PubMed ID: 37172566
[TBL] [Abstract][Full Text] [Related]
31. [Resection of navicular bone for severe midfoot deformity in children].
Laudrin P; Wicart P; Seringe R
Rev Chir Orthop Reparatrice Appar Mot; 2007 Sep; 93(5):478-85. PubMed ID: 17878839
[TBL] [Abstract][Full Text] [Related]
32. [Ritscher-Schinzel syndrome].
Matsumoto T; Kondoh T
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):587-8. PubMed ID: 11528910
[No Abstract] [Full Text] [Related]
33. Congenital talipes equinovarus (clubfoot): a disorder of the foot but not the hand.
Miedzybrodzka Z
J Anat; 2003 Jan; 202(1):37-42. PubMed ID: 12587918
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Generalized Verrucosis on a Background of 3C Syndrome Treated With Subcutaneous IgG Supplementation.
Fukaura R; Terashima-Murase C; Tanahashi K; Sato Y; Kawase M; Kato K; Akiyama M
JAMA Dermatol; 2023 Dec; 159(12):1397-1399. PubMed ID: 37851466
[TBL] [Abstract][Full Text] [Related]
36. The 6p subtelomere deletion syndrome.
DeScipio C
Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):377-82. PubMed ID: 17918735
[TBL] [Abstract][Full Text] [Related]
37. Current conservative management and classification of club foot: A review.
Balasankar G; Luximon A; Al-Jumaily A
J Pediatr Rehabil Med; 2016 Nov; 9(4):257-264. PubMed ID: 27935562
[TBL] [Abstract][Full Text] [Related]
38. Osteopathic manipulative treatment of congenital talipes equinovarus: a case report.
Andreoli E; Troiani A; Tucci V; Barlafante G; Cerritelli F; Pizzolorusso G; Renzetti C; Vanni D; Pantalone A; Salini V
J Bodyw Mov Ther; 2014 Jan; 18(1):4-10. PubMed ID: 24411143
[TBL] [Abstract][Full Text] [Related]
39. Gordon syndrome: literature review and a report of two cases.
Botha SJ; Bütow KW
Cleft Palate Craniofac J; 2015 Jan; 52(1):e18-22. PubMed ID: 24878349
[TBL] [Abstract][Full Text] [Related]
40. 3-C Ritscher-Schinzel syndrome with spinal subarachnoid cyst.
Sargar KM; Radmanesh A; Herman TE; Siegel MJ
J Perinatol; 2015 Mar; 35(3):233-4. PubMed ID: 25712599
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
