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Editorial

医学 儿科
作者
Victor A. McKusick
出处
期刊:Circulation [Ovid Technologies (Wolters Kluwer)]
卷期号:31 (1): 1-4 被引量:23
标识
DOI:10.1161/01.cir.31.1.1
摘要

HomeCirculationVol. 31, No. 1Editorial Free AccessResearch ArticlePDF/EPUBAboutView PDFSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessResearch ArticlePDF/EPUBEditorial The Genetic Mucopolysaccharidoses VICTOR A. MCKUSICK VICTOR A. MCKUSICKVICTOR A. MCKUSICK From the Division of Medical Genetics, Department of Medicine, Johns Hopkins University School of Medicine and Johns Hopkins Hospital, Baltimore, Maryland. Search for more papers by this author Originally published1 Jan 1965https://doi.org/10.1161/01.CIR.31.1.1Circulation. 1965;31:1–4 Previous Back to top Next FiguresReferencesRelatedDetailsCited By Hoover‐Fong J (2021) Current state of the art in treatment of Mendelian disease: Skeletal dysplasias, American Journal of Medical Genetics Part A, 10.1002/ajmg.a.62468, 185:11, (3359-3368), Online publication date: 1-Nov-2021. Rasmussen S, Pomputius A, Amberger J and Hamosh A (2021) Viewing Victor McKusick' s legacy through the lens of his bibliography , American Journal of Medical Genetics Part A, 10.1002/ajmg.a.62394, 185:11, (3212-3223), Online publication date: 1-Nov-2021. Misumi I, Chikazawa S, Ishitsu T, Higuchi S, Shimazu T, Ikeda C, Uchino M, Shibata Y, Ebihara K and Akahoshi R (2010) Atrioventricular Block and Diastolic Dysfunction in a Patient with Sanfilippo C, Internal Medicine, 10.2169/internalmedicine.49.4210, 49:21, (2313-2316), . Alturjuman A and Mehta A (2008) Mitral valvar prolapse and regurgitation combined with aortic regurgitation in a child with Sanfilippo syndrome type A, Cardiology in the Young, 10.1017/S1047951100006247, 8:2, (271-273), Online publication date: 1-Apr-1998. Roskamm H, Reindell H, Barmeyer J, Bubenheimer P, Gohlke-Bärwolf C, Gohlke H and Eichstädt H (1996) Aorteninsuffizienz Herzkrankheiten, 10.1007/978-3-642-97605-6_39, (1023-1050), . Fann J, Dalman R and Harris E (1993) Genetic and Metabolic Causes of Arterial Disease, Annals of Vascular Surgery, 10.1007/BF02000158, 7:6, (594-604), Online publication date: 1-Nov-1993. Reindell H, Roskamm H, Barmeyer J, Eichstädt H, Bubenheimer P, Gohlke H and Gohlke-Bärwolf C (1989) Aorteninsuffizienz Herzkrankheiten, 10.1007/978-3-642-97060-3_54, (1273-1298), . Spindola-Franco H and Fish B (1985) Valvular Heart Disease Radiology of the Heart, 10.1007/978-1-4613-8205-8_6, (179-258), . Barmeyer J, Roskamm H, Eichstädt H, Stürzenhofecker P, Reindell H, Bubenheimer P, Gohlke H and Gohlke-Bärwolf C (1982) Aorteninsuffizienz Herzkrankheiten, 10.1007/978-3-642-96617-0_48, (1291-1325), . Helmer F (1978) Die Anomalien des Einflußtraktes des rechten Ventrikels Herz und herznahe Gefäße, 10.1007/978-3-662-07751-1_5, (195-219), . Bolck F and Machnik G (1978) Die Leber Leber und Gallenwege, 10.1007/978-3-642-96410-7_1, (1-720), . Roskamm H, Reindell H, Barmeyer J, Wink K, Drägert W, Jaedicke W and Eichstädt H (1977) Die Aorteninsuffizienz Herzkrankheiten, 10.1007/978-3-642-96320-9_35, (741-762), . Patel V, Tappel A and O'Brien J (1970) Hyaluronidase and sulfatase deficiency in Hurler's syndrome, Biochemical Medicine, 10.1016/0006-2944(70)90037-2, 3:6, (447-457), Online publication date: 1-Jun-1970. Bigelow J and Starr A (1969) Multiple Valve Replacement American College of Surgeons / Deutsche Gesellschaft für Chirurgie, 10.1007/978-3-642-48257-1_17, (91-102), . Ross D, Gerbode F, Kerth W, Sanchez P, Puryear G, Bigelow J, Starr A, Muller W, Borst H and Schaudig A (1969) Cardiac Surgery Joint Meeting Munich 1968, 10.1007/978-3-642-49923-4_3, (76-112), . Fuhrmann W (1967) Genetic Aspects of Lipidoses Lipids and Lipidoses, 10.1007/978-3-642-87367-6_18, (490-528), . Langer L, Kronenberg R and Gorlin R (1966) A case simulating hurler syndrome of unusual longevity, without abnormal mucopolysacchariduria, The American Journal of Medicine, 10.1016/0002-9343(66)90139-2, 40:3, (448-457), Online publication date: 1-Mar-1966. FRASER G (1965) Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness, Annals of Human Genetics, 10.1111/j.1469-1809.1965.tb00512.x, 29:2, (171-196), Online publication date: 1-Nov-1965. Danes B and Bearn A (1965) Hurler's Syndrome: Demonstration of an Inherited Disorder of Connective Tissue in Cell Culture, Science, 10.1126/science.149.3687.987, 149:3687, (987-989), Online publication date: 27-Aug-1965. January 1, 1965Vol 31, Issue 1 Advertisement Article InformationMetrics © 1965 American Heart Association, Inc.https://doi.org/10.1161/01.CIR.31.1.1 Originally publishedJanuary 1, 1965 PDF download Advertisement
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