198 related articles for article (PubMed ID: 17688470)
1. Trichorhinophalangeal syndrome type II without the chromosome 8 deletion that resembled metachondromatosis.
Kikuchi N; Ogino T; Kashiwa H; Muragaki Y
Congenit Anom (Kyoto); 2007 Sep; 47(3):105-7. PubMed ID: 17688470
[TBL] [Abstract][Full Text] [Related]
2. Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864.
Herman TE; Chines A; McAlister WH; Gottesman GS; Eddy MC; Whyte MP
Pediatr Radiol; 1997 May; 27(5):436-41. PubMed ID: 9133359
[TBL] [Abstract][Full Text] [Related]
3. Trichorhinophalangeal syndrome type II presenting with short stature in a child.
Hazan F; Korkmaz HA; Yararbaş K; Wuyts W; Tükün A;
Arch Argent Pediatr; 2016 Dec; 114(6):e403-e407. PubMed ID: 27869420
[TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular characterization of a patient with Langer-Giedion syndrome and mosaic del(8)(q22.3q24.13).
Shanske AL; Patel A; Saukam S; Levy B; Lüdecke HJ
Am J Med Genet A; 2008 Dec; 146A(24):3211-6. PubMed ID: 19012352
[TBL] [Abstract][Full Text] [Related]
5. Trichorhinophalangeal syndrome, type II (Langer-Giedion syndrome).
Shin HT; Chang MW
Dermatol Online J; 2001 Dec; 7(2):8. PubMed ID: 12165224
[TBL] [Abstract][Full Text] [Related]
6. High-functioning autism in a Sri Lankan youth with Langer-Giedion syndrome.
Chandradasa M; Williams S
Psychiatr Genet; 2018 Jun; 28(3):55-57. PubMed ID: 29538090
[TBL] [Abstract][Full Text] [Related]
7. [Trichorhinophalangeal syndrome].
Dumić M; Ille J; Mikecin M; Cvitković M; Hitrec V; Potocki K
Lijec Vjesn; 1993; 115(5-6):163-5. PubMed ID: 8302139
[TBL] [Abstract][Full Text] [Related]
8. The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).
Le Merrer M; Ben Othmane K; Stanescu V; Lyonnet S; Van Maldergem L; Royer G; Munnich A; Maroteaux P
J Med Genet; 1992 Oct; 29(10):713-5. PubMed ID: 1433231
[TBL] [Abstract][Full Text] [Related]
9. [Langer-Giedion syndrome with 8q23.1-q24.12 deletion diagnosed by comparative genomic hybridization].
Ruiz-Botero F; Pachajoa H
Arch Argent Pediatr; 2016 Aug; 114(4):e228-32. PubMed ID: 27399022
[TBL] [Abstract][Full Text] [Related]
10. Langer-Giedion syndrome associated with submucous cleft palate.
Morioka D; Suse T; Shimizu Y; Ohkubo F; Hosaka Y
Plast Reconstr Surg; 1999 Apr; 103(5):1458-63. PubMed ID: 10190443
[TBL] [Abstract][Full Text] [Related]
11. Exostoses, enchondromatosis and metachondromatosis; diagnosis and management.
McFarlane J; Knight T; Sinha A; Cole T; Kiely N; Freeman R
Acta Orthop Belg; 2016 Mar; 82(1):102-5. PubMed ID: 26984661
[TBL] [Abstract][Full Text] [Related]
12. A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).
Hou J; Parrish J; Lüdecke HJ; Sapru M; Wang Y; Chen W; Hill A; Siegel-Bartelt J; Northrup H; Elder FF
Genomics; 1995 Sep; 29(1):87-97. PubMed ID: 8530105
[TBL] [Abstract][Full Text] [Related]
13. Crooked fingers and sparse hair: an interesting case of trichorhinophalangeal syndrome type 1.
Narayanan R; Chennareddy S
BMJ Case Rep; 2015 Jan; 2015():. PubMed ID: 25628322
[TBL] [Abstract][Full Text] [Related]
14. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy.
Chen CP; Lin SP; Liu YP; Chern SR; Wu PS; Su JW; Chen YT; Lee CC; Wang W
Gene; 2013 Oct; 529(1):176-80. PubMed ID: 23933416
[TBL] [Abstract][Full Text] [Related]
15. Trichorhinophalangeal syndrome type 2: another syndromic form of hydrometrocolpos.
Fryns JP
Am J Med Genet; 1997 Dec; 73(2):233. PubMed ID: 9409879
[No Abstract] [Full Text] [Related]
16. Trichorhinophalangeal syndrome type I--clinical, microscopic, and molecular features.
Jeon J; Kim JH; Oh CH
Indian J Dermatol Venereol Leprol; 2014; 80(1):54-7. PubMed ID: 24448126
[TBL] [Abstract][Full Text] [Related]
17. Case of meningothelial hamartoma with dermal melanocytosis in a patient with trichorhinophalangeal syndrome type II.
Kim GH; Lee JY; Yun SJ; Hong JS; Lee AY; Lee SH
J Dermatol; 2018 Nov; 45(11):e316-e317. PubMed ID: 29679406
[No Abstract] [Full Text] [Related]
18. Langer-Giedion syndrome with del 8 (q24.13-q24.22).
Okuno T; Inoue A; Asakura T; Nakao S
Clin Genet; 1987 Jul; 32(1):40-5. PubMed ID: 3502694
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletion of 8q. Occurrence in a patient with multiple exostoses and unusual facies.
Wilson WG; Wyandt HE; Shah H
Am J Dis Child; 1983 May; 137(5):444-8. PubMed ID: 6601906
[TBL] [Abstract][Full Text] [Related]
20. BMP-1 sublocalization on human chromosome 8. Molecular anatomy and orthopaedic implications.
Shore EM; Cook AL; Hahn GV; Kaplan FS; Wozney JM; Wagner MJ; Wells DE
Clin Orthop Relat Res; 1995 Feb; (311):199-209. PubMed ID: 7634576
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
