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24. ALBRIGHT'S HEREDITARY OSTEODYSTROPHY IN A MOTHER AND DAUGHTER. HINKLE DO; TRAVIS LB; DODGE WF Tex Rep Biol Med; 1965; 23():463-73. PubMed ID: 14336930 [No Abstract] [Full Text] [Related]
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26. 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]
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32. Gs(alpha) mutations and imprinting defects in human disease. Weinstein LS; Chen M; Liu J Ann N Y Acad Sci; 2002 Jun; 968():173-97. PubMed ID: 12119276 [TBL] [Abstract][Full Text] [Related]
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34. A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene. Germain-Lee EL; Schwindinger W; Crane JL; Zewdu R; Zweifel LS; Wand G; Huso DL; Saji M; Ringel MD; Levine MA Endocrinology; 2005 Nov; 146(11):4697-709. PubMed ID: 16099856 [TBL] [Abstract][Full Text] [Related]
35. 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]
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