BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 9138150)

  • 1. RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.
    Power MM; James RS; Barber JC; Fisher AM; Wood PJ; Leatherdale BA; Flanagan DE; Hatchwell E
    J Med Genet; 1997 Apr; 34(4):287-90. PubMed ID: 9138150
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype.
    Chassaing N; De Mas P; Tauber M; Vincent MC; Julia S; Bourrouillou G; Calvas P; Bieth E
    Am J Med Genet A; 2004 Aug; 128A(4):410-3. PubMed ID: 15264288
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Albright hereditary osteodystrophy and del(2) (q37.3) in four unrelated individuals.
    Phelan MC; Rogers RC; Clarkson KB; Bowyer FP; Levine MA; Estabrooks LL; Severson MC; Dobyns WB
    Am J Med Genet; 1995 Jul; 58(1):1-7. PubMed ID: 7573148
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype.
    Shrimpton AE; Braddock BR; Thomson LL; Stein CK; Hoo JJ
    Clin Genet; 2004 Dec; 66(6):537-44. PubMed ID: 15521982
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial Albright's hereditary osteodystrophy with hypoparathyroidism: normal structural Gs alpha gene.
    Shapira H; Friedman E; Mouallem M; Farfel Z
    J Clin Endocrinol Metab; 1996 Apr; 81(4):1660-2. PubMed ID: 8636385
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of two novel deletion mutations within the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy.
    Yu D; Yu S; Schuster V; Kruse K; Clericuzio CL; Weinstein LS
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3254-9. PubMed ID: 10487696
    [TBL] [Abstract][Full Text] [Related]  

  • 7. No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity.
    Izzi B; de Zegher F; Francois I; del Favero J; Goossens D; Wittevrongel C; Thys C; Van Geet C; Freson K
    J Hum Genet; 2012 Apr; 57(4):277-9. PubMed ID: 22277900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.
    Wilson LC; Leverton K; Oude Luttikhuis ME; Oley CA; Flint J; Wolstenholme J; Duckett DP; Barrow MA; Leonard JV; Read AP
    Am J Hum Genet; 1995 Feb; 56(2):400-7. PubMed ID: 7847374
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance.
    Elli FM; de Sanctis L; Madeo B; Maffini MA; Bordogna P; Pirelli A; Arosio M; Mantovani G
    Front Endocrinol (Lausanne); 2019; 10():604. PubMed ID: 31555217
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3.
    Elli FM; deSanctis L; Maffini MA; Bordogna P; Tessaris D; Pirelli A; Arosio M; Linglart A; Mantovani G
    Clin Epigenetics; 2019 Jan; 11(1):3. PubMed ID: 30616679
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy.
    Aldred MA; Aftimos S; Hall C; Waters KS; Thakker RV; Trembath RC; Brueton L
    Am J Med Genet; 2002 Nov; 113(2):167-72. PubMed ID: 12407707
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
    De Sanctis L; Romagnolo D; Olivero M; Buzi F; Maghnie M; Scirè G; Crino A; Baroncelli GI; Salerno M; Di Maio S; Cappa M; Grosso S; Rigon F; Lala R; De Sanctis C; Dianzani I
    Pediatr Res; 2003 May; 53(5):749-55. PubMed ID: 12621129
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of Albright's hereditary osteodystrophy-like syndrome complicated by several endocrinopathies: normal Gs alpha gene and chromosome 2q37.
    Sakaguchi H; Sanke T; Ohagi S; Iiri T; Nanjo K
    J Clin Endocrinol Metab; 1998 May; 83(5):1563-5. PubMed ID: 9589656
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A rare case of 2q37 microdeletion with Albright hereditary osteodystrophy-like phenotype.
    Simşek-Kiper PO; Utine GE; Alanay Y; Aktaş D; Alikaşifoğlu M; Boduroğlu K
    Turk J Pediatr; 2011; 53(5):558-60. PubMed ID: 22272459
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype.
    Bijlsma EK; Aalfs CM; Sluitjer S; Oude Luttikhuis ME; Trembath RC; Hoovers JM; Hennekam RC
    J Med Genet; 1999 Aug; 36(8):604-9. PubMed ID: 10465110
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Albright's hereditary osteodystrophy and pseudohypoparathyroidism.
    Wilson LC; Hall CM
    Semin Musculoskelet Radiol; 2002 Dec; 6(4):273-83. PubMed ID: 12541184
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.
    Polityko A; Maltseva O; Rumyantseva N; Khurs O; Seidel J; Claussen U; Weise A; Liehr T; Starke H
    Int J Mol Med; 2004 Dec; 14(6):977-9. PubMed ID: 15547662
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pseudohypoparathyroidism type Ia. Albright hereditary osteodystrophy: a model for research on G protein-coupled receptors and genomic imprinting.
    Simon A; Koppeschaar HP; Roijers JF; Höppener JW; Lips CJ
    Neth J Med; 2000 Mar; 56(3):100-9. PubMed ID: 10759021
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pseudohypoparathyroidism and GNAS epigenetic defects: clinical evaluation of albright hereditary osteodystrophy and molecular analysis in 40 patients.
    Mantovani G; de Sanctis L; Barbieri AM; Elli FM; Bollati V; Vaira V; Labarile P; Bondioni S; Peverelli E; Lania AG; Beck-Peccoz P; Spada A
    J Clin Endocrinol Metab; 2010 Feb; 95(2):651-8. PubMed ID: 20061437
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation.
    Klaassens M; Blom EW; Schrander JJ; Ris-Stalpers C; Nieuwenhuijzen Kruseman AC; van Steensel MA; Schrander-Stumpel CT
    Br J Dermatol; 2010 Mar; 162(3):690-4. PubMed ID: 19863504
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.