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Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C.
Clin Dysmorphol. 2016 Oct; 25(4):192-4.CD

Authors+Show Affiliations

aDepartment of Medical Genetics, Dr Faruk Sükan Maternity and Pediatric Hospital, Konya bDepartment of Medical Genetics, İstanbul Faculty of Medicine, İstanbul University, İstanbul, Turkey.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Letter

Language

eng

PubMed ID

27552067

Citation

Koçak Eker, Hatice, et al. "Holt-Oram Syndrome Because of the Novel TBX5 Mutation C.481A>C." Clinical Dysmorphology, vol. 25, no. 4, 2016, pp. 192-4.
Koçak Eker H, Altunoglu U, Toksoy G, et al. Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C. Clin Dysmorphol. 2016;25(4):192-4.
Koçak Eker, H., Altunoglu, U., Toksoy, G., & Kayserili, H. (2016). Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C. Clinical Dysmorphology, 25(4), 192-4. https://doi.org/10.1097/MCD.0000000000000121
Koçak Eker H, et al. Holt-Oram Syndrome Because of the Novel TBX5 Mutation C.481A>C. Clin Dysmorphol. 2016;25(4):192-4. PubMed PMID: 27552067.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C. AU - Koçak Eker,Hatice, AU - Altunoglu,Umut, AU - Toksoy,Güven, AU - Kayserili,Hülya, PY - 2016/8/24/entrez PY - 2016/8/24/pubmed PY - 2017/2/7/medline SP - 192 EP - 4 JF - Clinical dysmorphology JO - Clin. Dysmorphol. VL - 25 IS - 4 SN - 1473-5717 UR - https://www.unboundmedicine.com/medline/citation/27552067/Holt_Oram_syndrome_because_of_the_novel_TBX5_mutation_c_481A>C_ L2 - http://dx.doi.org/10.1097/MCD.0000000000000121 DB - PRIME DP - Unbound Medicine ER -