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Hyperkeratosis lenticularis perstans (Flegel) 持久性透镜性角化过度症(Flegel)
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00283773
E. Frenk, B. Tapernoux
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引用次数: 2
Beobachtungen zum Mosaizismus beim Cri-du-chat-Syndrom 图灵反应综合症
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00286761
W. Sachsse, E. Schmidt, E. Hellmich
{"title":"Beobachtungen zum Mosaizismus beim Cri-du-chat-Syndrom","authors":"W. Sachsse, E. Schmidt, E. Hellmich","doi":"10.1007/BF00286761","DOIUrl":"https://doi.org/10.1007/BF00286761","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"8 1","pages":"71-74"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00286761","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51204963","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}
引用次数: 1
Über die Verteilung der Gc-Typen in Südniedersachsen nebst Literaturübersicht über die Allelenhäufigkeit im deutschen Sprachgebiet 关于gc类型在下萨克森州的分布情况以及德语领域内的样式排序
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00281048
G. Jörgensen, P. Gabriel
{"title":"Über die Verteilung der Gc-Typen in Südniedersachsen nebst Literaturübersicht über die Allelenhäufigkeit im deutschen Sprachgebiet","authors":"G. Jörgensen, P. Gabriel","doi":"10.1007/BF00281048","DOIUrl":"https://doi.org/10.1007/BF00281048","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"1 1","pages":"602-606"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00281048","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51188143","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}
引用次数: 2
Biochemische Untersuchungen zur Frage der Existenz eines “silent Gene” im Polymorphismus der Pseudocholinesterasen 生化研究解释了伪证的食谱"银基因"的存在
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00281049
H. Goedde, D. Gehring, R. Hofmann
{"title":"Biochemische Untersuchungen zur Frage der Existenz eines “silent Gene” im Polymorphismus der Pseudocholinesterasen","authors":"H. Goedde, D. Gehring, R. Hofmann","doi":"10.1007/BF00281049","DOIUrl":"https://doi.org/10.1007/BF00281049","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"1 1","pages":"607-620"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00281049","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51188153","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}
引用次数: 2
Familiärer Minderwuchs mit unproportioniert hohen Wirbeln 家庭小弟弟没比例的卷柄
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00283975
W. Fuhrmann, E. Nägele, R. Gugler, E. Adili
{"title":"Familiärer Minderwuchs mit unproportioniert hohen Wirbeln","authors":"W. Fuhrmann, E. Nägele, R. Gugler, E. Adili","doi":"10.1007/BF00283975","DOIUrl":"https://doi.org/10.1007/BF00283975","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"16 1","pages":"271-282"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00283975","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51197298","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}
引用次数: 3
Untersuchungen von Proteinpolymorphismen an einer Familie mit gehäuften Chromosomenaberrationen 在一组有部分染色体遗体的染色体上发现了蛋白质多态性
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00286753
H. Ritter, W. Engel, J. Op't Hof, U. Wolf
{"title":"Untersuchungen von Proteinpolymorphismen an einer Familie mit gehäuften Chromosomenaberrationen","authors":"H. Ritter, W. Engel, J. Op't Hof, U. Wolf","doi":"10.1007/BF00286753","DOIUrl":"https://doi.org/10.1007/BF00286753","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"1 1","pages":"33-38"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00286753","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51204870","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}
引用次数: 1
Critical survey 重要的调查
Humangenetik Pub Date : 2004-01-01 DOI: 10.1007/BF00393993
W. Lenz
{"title":"Critical survey","authors":"W. Lenz","doi":"10.1007/BF00393993","DOIUrl":"https://doi.org/10.1007/BF00393993","url":null,"abstract":"","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"234 1","pages":"111-114"},"PeriodicalIF":0.0,"publicationDate":"2004-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00393993","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51212235","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}
引用次数: 97
The Bf locus in the HLA region of chromosome 6: linkage and association studies. 6号染色体HLA区Bf位点:连锁与关联研究。
Humangenetik Pub Date : 1975-12-23 DOI: 10.1007/BF00275141
B Olaisen, P Teisberg, T Gedde-Dahl, E Thorsby
{"title":"The Bf locus in the HLA region of chromosome 6: linkage and association studies.","authors":"B Olaisen,&nbsp;P Teisberg,&nbsp;T Gedde-Dahl,&nbsp;E Thorsby","doi":"10.1007/BF00275141","DOIUrl":"https://doi.org/10.1007/BF00275141","url":null,"abstract":"<p><p>Bf allele frequencies in a material of 172 unrelated Norwegians are given. Bf/HLA linkage relations in 49 informative matings with 178 children, and Bf/HLA association data of a material of 212 Bf-HLA haplotypes are presented. Of 171 informative meioses, there were no Bf-HLA-B recombinations, while 3 out of 158 Bf-HLA-A informative meioses showed recombination. There is significant association between the BfF and the HLA-BW35 allele. It is concluded that the Bf locus is situated on the HLA-B side of HLA-A within the HLA region, in very close proximity to HLA-B.</p>","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"30 4","pages":"291-6"},"PeriodicalIF":0.0,"publicationDate":"1975-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00275141","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12395804","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}
引用次数: 23
Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas. 脑肿瘤的细胞学和细胞遗传学研究。未发现22例单体脑膜瘤易位的证据。
Humangenetik Pub Date : 1975-12-23 DOI: 10.1007/BF00275149
H Zankl, A F Weiss, K D Zang
{"title":"Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.","authors":"H Zankl, A F Weiss, K D Zang","doi":"10.1007/BF00275149","DOIUrl":"10.1007/BF00275149","url":null,"abstract":"<p><p>The recently detected reciprocal translocations in chronic myeloic leucemia (CML) and Burkitt's lymphoma (BL) made it necessary to clarify if meningiomas really show the described monosomy 22 or also a translocation. In 10 out of 12 meningiomas a total or partial translocation of the missing chromosome 22 to another chromosome could be ruled out by fluorescence banding analysis. Two meningiomas showed marker chromosomes of such a complex composition that it was impossible to decide if a 22 translocation was present or not. From these results it was concluded that meningioma cells, in contrast to CML and BL, show almost regularly a loss of a definitive part of their genome.</p>","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"30 4","pages":"343-8"},"PeriodicalIF":0.0,"publicationDate":"1975-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12395810","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}
引用次数: 0
[Various banding simultaneously obtained on the same slides, after treatment by BrdU (author's transl)]. [经BrdU处理后，在同一张载玻片上同时获得多种条带（作者翻译）]。
Humangenetik Pub Date : 1975-12-23 DOI: 10.1007/BF00275142
Dutrillaux
{"title":"[Various banding simultaneously obtained on the same slides, after treatment by BrdU (author's transl)].","authors":"Dutrillaux","doi":"10.1007/BF00275142","DOIUrl":"10.1007/BF00275142","url":null,"abstract":"<p><p>A treatment by BrdU during 24 hrs, followed by a treatment by thymidine, during 30 hrs, induces in the same preparations, many types of chromosome banding R-, Q-, H-bands, and several types of asymmetry. This indicates that the BrdU is not incorporated only in some parts of the karyotype, but, on the contrary, any where, and then induces different banding according to the site of its incorporation. Above all, the type of band is determined by the period of the phase S in which the cell was at the time of the treatment by BrdU. Thus the coexistence of many types of banding may be explained here by the great variability of the cellular cycle of the lymphocytes in culture.</p>","PeriodicalId":75916,"journal":{"name":"Humangenetik","volume":"30 4","pages":"297-306"},"PeriodicalIF":0.0,"publicationDate":"1975-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11278343","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}
引用次数: 0
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