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Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation.
J Eur Acad Dermatol Venereol. 2010 Aug; 24(8):974-5.JE

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Letter

Language

eng

PubMed ID

20015054

Citation

Alvarez, F, et al. "Albright Hereditary Osteodystrophy: Report of a Particular Clinical Phenotype Caused By a Novel GNAS Mutation." Journal of the European Academy of Dermatology and Venereology : JEADV, vol. 24, no. 8, 2010, pp. 974-5.
Alvarez F, Kottler ML, Paul C, et al. Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation. J Eur Acad Dermatol Venereol. 2010;24(8):974-5.
Alvarez, F., Kottler, M. L., Paul, C., Gennero, I., Salles, J. P., & Mazereeuw-Hautier, J. (2010). Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation. Journal of the European Academy of Dermatology and Venereology : JEADV, 24(8), 974-5. https://doi.org/10.1111/j.1468-3083.2009.03539.x
Alvarez F, et al. Albright Hereditary Osteodystrophy: Report of a Particular Clinical Phenotype Caused By a Novel GNAS Mutation. J Eur Acad Dermatol Venereol. 2010;24(8):974-5. PubMed PMID: 20015054.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation. AU - Alvarez,F, AU - Kottler,M L, AU - Paul,C, AU - Gennero,I, AU - Salles,J P, AU - Mazereeuw-Hautier,J, Y1 - 2009/12/15/ PY - 2009/12/18/entrez PY - 2009/12/18/pubmed PY - 2010/12/17/medline SP - 974 EP - 5 JF - Journal of the European Academy of Dermatology and Venereology : JEADV JO - J Eur Acad Dermatol Venereol VL - 24 IS - 8 SN - 1468-3083 UR - https://www.unboundmedicine.com/medline/citation/20015054/Albright_hereditary_osteodystrophy:_report_of_a_particular_clinical_phenotype_caused_by_a_novel_GNAS_mutation_ L2 - https://doi.org/10.1111/j.1468-3083.2009.03539.x DB - PRIME DP - Unbound Medicine ER -