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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 24473423)

  • 21. 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]  

  • 22. Prenatal onset GAPO syndrome with a novel ANTXR1 variant in an Indian child: Expansion of the phenotype & literature review.
    Balakrishnan S; Goud I; Teegala ML
    Eur J Med Genet; 2024 Apr; 68():104929. PubMed ID: 38423276
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mutations in ANTXR1 cause GAPO syndrome.
    Stránecký V; Hoischen A; Hartmannová H; Zaki MS; Chaudhary A; Zudaire E; Nosková L; Barešová V; Přistoupilová A; Hodaňová K; Sovová J; Hůlková H; Piherová L; Hehir-Kwa JY; de Silva D; Senanayake MP; Farrag S; Zeman J; Martásek P; Baxová A; Afifi HH; St Croix B; Brunner HG; Temtamy S; Kmoch S
    Am J Hum Genet; 2013 May; 92(5):792-9. PubMed ID: 23602711
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Distribution of
    Gupta V; Panigrahi A; Somarajan BI; Gupta S; Tripathy K; Singh A; Sharma A; Tandon R; Pradhan D; Sharma A; Kushwaha T; Inampudi KK
    Mol Vis; 2023; 29():365-377. PubMed ID: 38577561
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.
    Przyklenk M; Karmacharya S; Bonasera D; Pasanen-Zentz AL; Kmoch S; Paulsson M; Wagener R; Liccardi G; Schiavinato A
    Sci Rep; 2024 Apr; 14(1):9321. PubMed ID: 38653789
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [Ophthalmological anomalies of the GAPO syndrome (growth retardation, alopecia, pseudo-anodontia, optic atrophy). Apropos of a case].
    Dellac M; Manouvrier-Hanu S; Rouland JF
    J Fr Ophtalmol; 1990; 13(11-12):547-50. PubMed ID: 2081845
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Value of imaging in GAPO syndrome].
    Goucha S; Mnif N; Bouhala T; Tenzakhti F; El Andaloussi H; Fazaa B; Hamza R; Kamoun MR
    J Radiol; 2002 Feb; 83(2 Pt 1):153-6. PubMed ID: 11965163
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Two siblings with GAPO syndrome: Ophthalmic presentation and histopathologic findings.
    Falcone MM; Chang YH; Lidov H; Stagner AM; Dagi LR
    Ophthalmic Genet; 2023 Dec; 44(6):598-601. PubMed ID: 36748830
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. GAPO syndrome: first patients with partially empty sella.
    Orbak Z; Orbak R; Ozkan B; Okten A
    J Pediatr Endocrinol Metab; 2002 Jun; 15(6):865-8. PubMed ID: 12099399
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Tooth eruption disturbances and syndromes].
    Oosterkamp BC; Ockeloen CW; Carels CE; Kuijpers-Jagtman AM
    Ned Tijdschr Tandheelkd; 2014 Apr; 121(4):233-8. PubMed ID: 24881265
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Converging physiological roles of the anthrax toxin receptors.
    Sergeeva OA; van der Goot FG
    F1000Res; 2019; 8():. PubMed ID: 31448094
    [TBL] [Abstract][Full Text] [Related]  

  • 38. GAPO syndrome: report on the first case in Japan.
    Moriya N; Mitsui T; Shibata T; Yamaguchi K; Kanazawa C; Matsunaga A; Hayasaka K
    Am J Med Genet; 1995 Sep; 58(3):257-61. PubMed ID: 8533828
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Two siblings with GAPO syndrome: a novel missense variant in ANTXR1.
    Yildiz O; Taşdelen E; Karakaya T; Taşdelen H
    Clin Dysmorphol; 2022 Oct; 31(4):191-195. PubMed ID: 36094357
    [No Abstract]   [Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.