Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultationHow to cite this article: Li Y, Steinberg AG, Bain L, Yaeger D, Bieler A, Ewing R, Kaimal G, Krantz I. 2007. Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultation. Am J Med Genet Part A 143A:1546–1553.

Autor: Li, Yuelin, Steinberg, Annie G., Bain, Lisa, Yaeger, Dinah, Bieler, Ari, Ewing, Rachel, Kaimal, Girija, Krantz, Ian

Publikováno v: American Journal of Medical Genetics. Part A; July 2007, Vol. 143 Issue: 14 p1546-1553, 8p

HLA B27 in Ankylosing Spondylitis: Differences in Frequency and Relative Risk in American Blacks and Caucasians.

Autor: Khan MA; From the Department of Medicine, Cleveland Metropolitan General Hospital; the Division of Human Genetics, Case Western Reserve University; and the Department of Immunoputhology, the Cleveland Clinic, Cleveland, Ohio., Braun WE; From the Department of Medicine, Cleveland Metropolitan General Hospital; the Division of Human Genetics, Case Western Reserve University; and the Department of Immunoputhology, the Cleveland Clinic, Cleveland, Ohio., Kushner I; From the Department of Medicine, Cleveland Metropolitan General Hospital; the Division of Human Genetics, Case Western Reserve University; and the Department of Immunoputhology, the Cleveland Clinic, Cleveland, Ohio., Grecek DE; From the Department of Medicine, Cleveland Metropolitan General Hospital; the Division of Human Genetics, Case Western Reserve University; and the Department of Immunoputhology, the Cleveland Clinic, Cleveland, Ohio., Muir WA; From the Department of Medicine, Cleveland Metropolitan General Hospital; the Division of Human Genetics, Case Western Reserve University; and the Department of Immunoputhology, the Cleveland Clinic, Cleveland, Ohio., Steinberg AG; From the Department of Medicine, Cleveland Metropolitan General Hospital; the Division of Human Genetics, Case Western Reserve University; and the Department of Immunoputhology, the Cleveland Clinic, Cleveland, Ohio.

Publikováno v: The Journal of rheumatology [J Rheumatol] 2023 Jan; Vol. 50 (1), pp. 39-43.

Proliferative Glomerulonephritis With Fibrils, Monoclonal κ Light Chain, and C3 Deposits.

Autor: Steinberg AG; Department of Nephrology, Royal Melbourne Hospital, Parkville, Victoria, Australia. Electronic address: adam.steinberg@mh.org.au., Fox LC; Peter MacCallum Cancer Centre, Parkville, Victoria, Australia., Bender S; Centre National de la Recherche Scientifique UMR CNRS 7276/INSERM U1262, Université de Limoges, Limoges, France., Batrouney A; Department of Anatomical Pathology, Royal Melbourne Hospital, Parkville, Victoria, Australia., Juneja S; Department of Hematology, Royal Melbourne Hospital, Parkville, Victoria, Australia., Sirac C; Centre National de la Recherche Scientifique UMR CNRS 7276/INSERM U1262, Université de Limoges, Limoges, France., Touchard G; Service de Néphrologie, Hémodialyse et Transplantation Rénale, CIC INSERM 1402, Centre de référence pour l'amylose AL et autres maladies par dépôt d'immunoglobulines monoclonales, CHU Poitiers, Poitiers, France., Blombery P; Peter MacCallum Cancer Centre, Parkville, Victoria, Australia., Finlay MJ; Department of Anatomical Pathology, Royal Melbourne Hospital, Parkville, Victoria, Australia; Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Melbourne, Victoria, Australia., Bridoux F; Centre National de la Recherche Scientifique UMR CNRS 7276/INSERM U1262, Université de Limoges, Limoges, France; Service de Néphrologie, Hémodialyse et Transplantation Rénale, CIC INSERM 1402, Centre de référence pour l'amylose AL et autres maladies par dépôt d'immunoglobulines monoclonales, CHU Poitiers, Poitiers, France., Barbour TD; Department of Nephrology, Royal Melbourne Hospital, Parkville, Victoria, Australia; Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Melbourne, Victoria, Australia.

Publikováno v: American journal of kidney diseases : the official journal of the National Kidney Foundation [Am J Kidney Dis] 2021 Sep; Vol. 78 (3), pp. 459-463. Date of Electronic Publication: 2021 Mar 25.

儿童遗传性胰腺炎的研究进展.

Autor: 于晓政¹, 吴 捷¹ wujie@bch.com.cn

Publikováno v: Journal of Clinical Hepatology / Linchuang Gandanbing Zazhi. Aug2024, Vol. 40 Issue 8, p1709-1714. 6p.

The expression and interaction of hereditary factors affecting hair growth in mice; external observations

Autor: Steinberg Ag, Fraser Fc

Publikováno v: Canadian journal of research. 24

Macroscopic observations on the expression of two mutant alleles ("hairless" and "rhino") in the house mouse, and on their interaction with one another and with a third mutation ("Naked") producing hypotrichosis of a different type, have been describ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7728a7552f5f6ec0a0cdea216f3d8d2
https://pubmed.ncbi.nlm.nih.gov/21066139