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[Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier].
Rev Esp Cardiol 2011; 64(12):1225-6RE

Authors

No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Letter

Language

spa

PubMed ID

21752519

Citation

Murga-Eizagaechevarria, Nekane, et al. "[Holt-Oram Syndrome: Family Affected Without TBX5 Mutation and Without Phenotype Manifestations in a Probable Mutation Carrier]." Revista Espanola De Cardiologia, vol. 64, no. 12, 2011, pp. 1225-6.
Murga-Eizagaechevarria N, Garcia-Barcina M, Sarasola Diez E. [Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier]. Rev Esp Cardiol. 2011;64(12):1225-6.
Murga-Eizagaechevarria, N., Garcia-Barcina, M., & Sarasola Diez, E. (2011). [Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier]. Revista Espanola De Cardiologia, 64(12), pp. 1225-6. doi:10.1016/j.recesp.2011.02.016.
Murga-Eizagaechevarria N, Garcia-Barcina M, Sarasola Diez E. [Holt-Oram Syndrome: Family Affected Without TBX5 Mutation and Without Phenotype Manifestations in a Probable Mutation Carrier]. Rev Esp Cardiol. 2011;64(12):1225-6. PubMed PMID: 21752519.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier]. AU - Murga-Eizagaechevarria,Nekane, AU - Garcia-Barcina,Maria, AU - Sarasola Diez,Esther, Y1 - 2011/07/12/ PY - 2010/10/27/received PY - 2011/02/08/accepted PY - 2011/7/15/entrez PY - 2011/7/15/pubmed PY - 2012/3/21/medline SP - 1225 EP - 6 JF - Revista espanola de cardiologia JO - Rev Esp Cardiol VL - 64 IS - 12 SN - 1579-2242 UR - https://www.unboundmedicine.com/medline/citation/21752519/[Holt_Oram_syndrome:_family_affected_without_TBX5_mutation_and_without_phenotype_manifestations_in_a_probable_mutation_carrier]_ L2 - http://www.revespcardiol.org/en/linksolver/ft/pii/S0300-8932(11)00380-0 DB - PRIME DP - Unbound Medicine ER -