المؤلفون: Guo DC; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Duan X; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Mimnagh K; Department of Internal Medicine, WVU School of Medicine-Charleston Division (Retired), Morgantown, West Virginia, USA., Cecchi AC; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Marin IC; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Yu Y; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Velasco WV; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Lee K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Zhu X; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Murdock DR; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Leal SM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Wheeler MM; Genome Sciences, University of Washington, Seattle, Washington, USA., Smith J; Genome Sciences, University of Washington, Seattle, Washington, USA., Bamshad MJ; Genome Sciences, University of Washington, Seattle, Washington, USA., Milewicz DM; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.

المصدر: Clinical genetics [Clin Genet] 2023 Jun; Vol. 103 (6), pp. 704-708. Date of Electronic Publication: 2023 Mar 07.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

مواضيع طبية MeSH: Marfan Syndrome*/genetics , Aortic Diseases*, Humans ; Fibrillin-1/genetics ; Mutation ; Phenotype

المؤلفون: Boerio ML; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX (M.L.B., I.C.M., A.P., D.G., S.K.P., D.M.M.)., Engelhardt NM; Division of Human Genetics, Children's Hospital of Philadelphia, PA (N.M.E., S.C., J.I.G.)., Cuddapah S; Division of Human Genetics, Children's Hospital of Philadelphia, PA (N.M.E., S.C., J.I.G.)., Gold JI; Division of Human Genetics, Children's Hospital of Philadelphia, PA (N.M.E., S.C., J.I.G.)., Marin IC; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX (M.L.B., I.C.M., A.P., D.G., S.K.P., D.M.M.)., Pinard A; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX (M.L.B., I.C.M., A.P., D.G., S.K.P., D.M.M.)., Guo D; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX (M.L.B., I.C.M., A.P., D.G., S.K.P., D.M.M.)., Prakash SK; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX (M.L.B., I.C.M., A.P., D.G., S.K.P., D.M.M.)., Milewicz DM; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, TX (M.L.B., I.C.M., A.P., D.G., S.K.P., D.M.M.).

المصدر: Circulation. Genomic and precision medicine [Circ Genom Precis Med] 2022 Dec; Vol. 15 (6), pp. e003707. Date of Electronic Publication: 2022 Nov 09.

نوع المنشور: Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101714113 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2574-8300 (Electronic) Linking ISSN: 25748300 NLM ISO Abbreviation: Circ Genom Precis Med Subsets: MEDLINE

مواضيع طبية MeSH: Aortic Aneurysm, Thoracic* , Aortic Diseases*/genetics, Humans ; Aorta ; Ubiquitin-Protein Ligases

المؤلفون: Marin IC; CardioVital Investigaciones, Medellin, Colombia., Velasquez CA; CardioVital Investigaciones, Medellin, Colombia., Cardona-Velez J; CardioVital Investigaciones, Medellin, Colombia., Jaramillo V; CardioVital Investigaciones, Medellin, Colombia; Universidad CES, Medellin, Colombia., Alviar CL; Cleveland Clinic Foundation, Cleveland, OH., Jaramillo NI; CardioVital Investigaciones, Medellin, Colombia; Cardiology, Clinica Las Americas, Medellin, Colombia.

المصدر: Journal of the American Society of Hypertension : JASH [J Am Soc Hypertens] 2016 Jul; Vol. 10 Suppl 1, pp. e8.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 101312518 Publication Model: Print Cited Medium: Internet ISSN: 1878-7436 (Electronic) Linking ISSN: 18787436 NLM ISO Abbreviation: J Am Soc Hypertens Subsets: PubMed not MEDLINE