151 related articles for article (PubMed ID: 18470892)
1. GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature.
Goloni-Bertollo EM; Ruiz MT; Goloni CB; Muniz MP; Valério NI; Pavarino-Bertelli EC
Am J Med Genet A; 2008 Jun; 146A(12):1523-9. PubMed ID: 18470892
[TBL] [Abstract][Full Text] [Related]
2. Ophthalmic aspects of GAPO syndrome: case report and review.
Rim PH; Marques-de-Faria AP
Ophthalmic Genet; 2005 Sep; 26(3):143-7. PubMed ID: 16272061
[TBL] [Abstract][Full Text] [Related]
3. Ophthalmic findings in GAPO syndrome.
Ilker SS; Oztürk F; Kurt E; Temel M; Gül D; Sayli BS
Jpn J Ophthalmol; 1999; 43(1):48-52. PubMed ID: 10197743
[TBL] [Abstract][Full Text] [Related]
4. GAPO syndrome: a new case.
Sandgren G
Am J Med Genet; 1995 Jul; 58(1):87-90. PubMed ID: 7573163
[TBL] [Abstract][Full Text] [Related]
5. GAPO syndrome: a new case of this rare syndrome and a review of the relative importance of different phenotypic features in diagnosis.
Bacon W; Hall RK; Roset JP; Boukari A; Tenenbaum H; Walter B
J Craniofac Genet Dev Biol; 1999; 19(4):189-200. PubMed ID: 10731088
[TBL] [Abstract][Full Text] [Related]
6. [The GAPO syndrome (growth retardation, alopecia, pseudo-anodontia, optic atrophy). A new case report].
Manouvrier-Hanu S; Largillière C; Farriaux JP
J Genet Hum; 1988 Aug; 36(4):373-8. PubMed ID: 3065457
[No Abstract] [Full Text] [Related]
7. GAPO syndrome: four new patients with congenital glaucoma and myelinated retinal nerve fiber layer.
Bozkurt B; Yildirim MS; Okka M; Bitirgen G
Am J Med Genet A; 2013 Apr; 161A(4):829-34. PubMed ID: 23494824
[TBL] [Abstract][Full Text] [Related]
8. GAPO syndrome with pansutural craniosynostosis leading to intracranial hypertension.
Goyal N; Gurjar H; Sharma BS; Tripathi M; Chandra PS
BMJ Case Rep; 2014 Jan; 2014():. PubMed ID: 24473423
[TBL] [Abstract][Full Text] [Related]
9. GAPO syndrome: a report of two siblings and a review of literature.
Nanda A; Al-Ateeqi WA; Al-Khawari MA; Alsaleh QA; Anim JT
Pediatr Dermatol; 2010; 27(2):156-61. PubMed ID: 20537066
[TBL] [Abstract][Full Text] [Related]
10. Growth retardation, alopecia, pseudoanodontia, and optic atrophy (GAPO syndrome) with congenital glaucoma.
Mullaney PB; Jacquemin C; al-Rashed W; Smith W
Arch Ophthalmol; 1997 Jul; 115(7):940-1. PubMed ID: 9230846
[No Abstract] [Full Text] [Related]
11. Dental findings in GAPO syndrome: case report.
da Silveira HE; Quadros OF; Dalla-Bona RR; da Silveira HL; Fritscher GG
Braz Dent J; 2006; 17(3):259-62. PubMed ID: 17262136
[TBL] [Abstract][Full Text] [Related]
12. Changing facial features in a child with GAPO syndrome caused by novel mutation in the ANTXR1 gene and uniparental disomy of chromosome 2.
Smigiel R; Rozensztrauch A; Walczak A; Rydzanicz M; Stawinski P; Berghausen-Mazur M; Kostrzewa G; Sasiadek M; Ploski R
Clin Dysmorphol; 2019 Oct; 28(4):211-214. PubMed ID: 31425299
[No Abstract] [Full Text] [Related]
13. GAPO Syndrome-A Rare Cause of Osteomyelitis of Jaws; Report of 4 Cases With a Brief Review of the Literature.
Puranik RS; Puranik SR; Hallur N; Venkatesh D
J Oral Maxillofac Surg; 2018 Jun; 76(6):1216-1225. PubMed ID: 29304326
[TBL] [Abstract][Full Text] [Related]
14. Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome.
Bayram Y; Pehlivan D; Karaca E; Gambin T; Jhangiani SN; Erdin S; Gonzaga-Jauregui C; Wiszniewski W; Muzny D; ; Elcioglu NH; Yildirim MS; Bozkurt B; Zamani AG; Boerwinkle E; Gibbs RA; Lupski JR
Am J Med Genet A; 2014 Sep; 164A(9):2328-34. PubMed ID: 25045128
[TBL] [Abstract][Full Text] [Related]
15. GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.
Abdel-Hamid MS; Ismail S; Zaki MS; Abdel-Salam GMH; Otaify GA; Issa MY; Abdel-Kader M; Girgis M; Aboul-Ezz E; Mazen I; Aglan MS; Temtamy SA
Am J Med Genet A; 2019 Feb; 179(2):237-242. PubMed ID: 30575274
[TBL] [Abstract][Full Text] [Related]
16. GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the older.
Wajntal A; Koiffmann CP; Mendonça BB; Epps-Quaglia D; Sotto MN; Rati PB; Opitz JM
Am J Med Genet; 1990 Oct; 37(2):213-23. PubMed ID: 2248288
[TBL] [Abstract][Full Text] [Related]
17. Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
Tipton RE; Gorlin RJ
Am J Med Genet; 1984 Oct; 19(2):209-16. PubMed ID: 6507471
[TBL] [Abstract][Full Text] [Related]
18. GAPO syndrome: report of three affected brothers.
Gagliardi AR; González CH; Pratesi R
Am J Med Genet; 1984 Oct; 19(2):217-23. PubMed ID: 6507472
[TBL] [Abstract][Full Text] [Related]
19. [Ocular manifestation in GAPO syndrome. Report of the first tunisian case].
Touzri RA; Goucha S; Kriaa L; Beltaif O; Fazaa B; El Andolsi H; Kamoun MR; Ouertani A
J Fr Ophtalmol; 2003 Dec; 26(10):1067-70. PubMed ID: 14691402
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation at ANTXR1 in an Indian patient with growth retardation-alopecia-pseudoanodontia-optic atrophy syndrome.
Chattopadhyay E; Ghose S; Ray A; Anjum N; Mazumdar A; Roy B
Oral Surg Oral Med Oral Pathol Oral Radiol; 2017 Nov; 124(5):e261-e265. PubMed ID: 28870703
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
