184 related articles for article (PubMed ID: 27048037)
1. Holt Oram syndrome: a case report and review of the literature.
Virdis G; Dessole M; Dessole S; Ambrosini G; Cosmi E; Cherchil PL; Capobianco G
Clin Exp Obstet Gynecol; 2016; 43(1):137-9. PubMed ID: 27048037
[TBL] [Abstract][Full Text] [Related]
2. An Unusual Finding of a Double Orifice Mitral Valve in a Patient With Holt-Oram Syndrome.
Verma KP; Healy S; Teng J; Nerlekar N
Heart Lung Circ; 2019 Apr; 28(4):e99-e100. PubMed ID: 30555010
[No Abstract] [Full Text] [Related]
3. Type-I umbilical-systemic shunt with abnormal connection to azygos vein in fetus with de-novo TBX5 mutation related to Holt-Oram syndrome.
Achiron R; Har-Toov J; Kivilevitch Z
Ultrasound Obstet Gynecol; 2024 May; 63(5):709-711. PubMed ID: 38197531
[No Abstract] [Full Text] [Related]
4. Malignant hyperthermia-like manifestations in a two-month-old child with Holt-Oram syndrome undergoing cardiac surgery.
Franklin AD; Lorinc AN; Donahue BS
J Cardiothorac Vasc Anesth; 2014 Oct; 28(5):1326-7. PubMed ID: 24011877
[No Abstract] [Full Text] [Related]
5. Familial dilated cardiomyopathy associated with pathogenic TBX5 variants: Expanding the cardiac phenotype associated with Holt-Oram syndrome.
Patterson J; Coats C; McGowan R
Am J Med Genet A; 2020 Jul; 182(7):1725-1734. PubMed ID: 32449309
[TBL] [Abstract][Full Text] [Related]
6. Findings in a patient with Wildervanck syndrome.
Dimitriadis PA; Mackeith S; Archibald C; Hussain S; Mansell N
Clin Neuroradiol; 2015 Mar; 25(1):69-71. PubMed ID: 24997129
[No Abstract] [Full Text] [Related]
7. Rare cardiac defect in Holt-Oram syndrome.
Sinha R; Nema C
Cardiovasc J Afr; 2012 Mar; 23(2):e3-4. PubMed ID: 22447508
[TBL] [Abstract][Full Text] [Related]
8. Holt-Oram syndrome: a case report.
Chin J; Pereira S; Camacho A; Pessoa B; Bento D; Amado J; Pereira J; de Jesus I
Rev Port Cardiol; 2014 Nov; 33(11):737.e1-5. PubMed ID: 25455949
[TBL] [Abstract][Full Text] [Related]
9. Holt-Oram syndrome: contribution of prenatal 3-dimensional sonography in an index case.
Sepulveda W; Enriquez G; Martinez JL; Mejia R
J Ultrasound Med; 2004 Jul; 23(7):983-7. PubMed ID: 15292570
[No Abstract] [Full Text] [Related]
10. Micromelic upper limbs and cardiac defect: A fetal case of Holt-Oram syndrome identified in the first trimester.
Han J; Zhen L; Li R; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2021 Mar; 258():471-473. PubMed ID: 33495059
[No Abstract] [Full Text] [Related]
11. Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray.
Stipoljev F; Miric-Tesanic D; Hafner T; Barbalic M; Logara M; Lasan-Trcic R; Vicic A; Gjergja-Juraski R
Eur J Med Genet; 2017 Nov; 60(11):589-594. PubMed ID: 28807863
[TBL] [Abstract][Full Text] [Related]
12. Novel TBX5 duplication in a Japanese family with Holt-Oram syndrome.
Kimura M; Kikuchi A; Ichinoi N; Kure S
Pediatr Cardiol; 2015 Jan; 36(1):244-7. PubMed ID: 25274398
[TBL] [Abstract][Full Text] [Related]
13. [Holt-Oram syndrome: genetic counseling and diagnosis with prenatal ultrasonography].
Pete B; Harmath A; Szigeti Z; Papp C; Hajdú J
Orv Hetil; 2007 Nov; 148(46):2173-6. PubMed ID: 17988974
[TBL] [Abstract][Full Text] [Related]
14. Defining Features of the Upper Extremity in Holt-Oram Syndrome.
Wall LB; Piper SL; Habenicht R; Oishi SN; Ezaki M; Goldfarb CA
J Hand Surg Am; 2015 Sep; 40(9):1764-8. PubMed ID: 26243320
[TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
Jhang WK; Lee BH; Kim GH; Lee JO; Yoo HW
Cardiol Young; 2015 Aug; 25(6):1093-8. PubMed ID: 25216260
[TBL] [Abstract][Full Text] [Related]
16. Unexplained right atrial enlargement may be a sign of Holt-Oram syndrome in the fetus.
Paladini D; Tiesi M; Buffi D; Tuo G; Marasini M
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):475-6. PubMed ID: 24185902
[TBL] [Abstract][Full Text] [Related]
17. [Holt-Oram syndrome associated with facial anomalies. A case report].
Aviña-Fierro JA; Colonnelli-Barba G
Rev Med Inst Mex Seguro Soc; 2010; 48(6):657-9. PubMed ID: 21184723
[TBL] [Abstract][Full Text] [Related]
18. TBX3 and TBX5 duplication: A family with an atypical overlapping Holt-Oram/ulnar-mammary syndrome phenotype.
Cenni C; Andres S; Hempel M; Strom TM; Thomas E; Davies A; Timoney N; Frigiola A; Logan M; Holder-Espinasse M
Eur J Med Genet; 2021 Jul; 64(7):104213. PubMed ID: 33930582
[TBL] [Abstract][Full Text] [Related]
19. Prenatal sonographic diagnosis of familial Holt-Oram syndrome associated with type B interrupted aortic arch.
Law KM; Tse KT
Hong Kong Med J; 2008 Aug; 14(4):317-20. PubMed ID: 18685167
[TBL] [Abstract][Full Text] [Related]
20. A new mutation in the TBX5 gene in Holt-Oram syndrome: two cases in the same family and prenatal diagnosis.
Atik T; Dervisoglu H; Onay H; Ozkinay F; Cogulu O
J Trop Pediatr; 2014 Jun; 60(3):257-9. PubMed ID: 24408148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]