{"title":"Zur Populationsgenetik der Adenylatkinase: Genhäufigkeit in einer südwestdeutschen Stichprobe","authors":"B. Wille, H. Ritter","doi":"10.1007/BF00281967","DOIUrl":"https://doi.org/10.1007/BF00281967","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"5 1","pages":"278-280"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00281967","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51193748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Mit einem alkylierenden Agens (Zitostop) in vitro induzierbare Mutationen bei Malignomen und bei Syndromen, die zur Malignität disponieren","authors":"D. Schuler, G. Fekete, M. Dobos","doi":"10.1007/BF00283981","DOIUrl":"https://doi.org/10.1007/BF00283981","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"16 1","pages":"329-336"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00283981","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51196872","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Zur frage der unterschiedlichen Verteilung der ABO-Blutgruppen bei erst-und nachgeborenen Kindern","authors":"W. Kircher","doi":"10.1007/BF00283984","DOIUrl":"https://doi.org/10.1007/BF00283984","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"16 1","pages":"345-347"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00283984","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51196880","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Zum Polymorphismus der Glutamat-Pyruvat-Transaminase (GPT) menschlicher Erythrocyten in Westdeutschland","authors":"H. Hellenbroich, B. G. Potrafki, G. Pulverer","doi":"10.1007/BF00283986","DOIUrl":"https://doi.org/10.1007/BF00283986","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"16 1","pages":"351-353"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00283986","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51196897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Serumgruppen und Krankheit","authors":"G. Wendt, J. Krüger, I. Kindermann","doi":"10.1007/BF00286797","DOIUrl":"https://doi.org/10.1007/BF00286797","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"6 1","pages":"281-299"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00286797","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51205567","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Chromosomenmosaik 46,XY,D-,t(DqGq)+/92,XYXY,2D-,2t(DqGq)+ bei einem Säugling mit Down-Syndrom","authors":"H. Waller, M. Waller","doi":"10.1007/BF00277905","DOIUrl":"https://doi.org/10.1007/BF00277905","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"17 1","pages":"99-104"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00277905","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51182647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
U. Wolf, H. Reinwein, Renate Porsch, R. Schröter, H. Baitsch
{"title":"Defizienz an den kurzen Armen eines Chromosomes Nr. 4","authors":"U. Wolf, H. Reinwein, Renate Porsch, R. Schröter, H. Baitsch","doi":"10.1007/BF00279119","DOIUrl":"https://doi.org/10.1007/BF00279119","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"1 1","pages":"397-413"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00279119","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51183897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Consanguinité et effectifs de la population des communes","authors":"A. Leguèbe","doi":"10.1007/BF00281955","DOIUrl":"https://doi.org/10.1007/BF00281955","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"5 1","pages":"197-200"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00281955","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51193562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
G. Schwanitz, M. Reither, G. Grosse, C. Hägele, K. Grosse, U. Gutfried
{"title":"Partial monosomy 13 as the result of a balanced translocation 3/13 pat","authors":"G. Schwanitz, M. Reither, G. Grosse, C. Hägele, K. Grosse, U. Gutfried","doi":"10.1007/BF00394200","DOIUrl":"https://doi.org/10.1007/BF00394200","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"29 1","pages":"354"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00394200","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51212316","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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