Jinrui idengaku zasshi. The Japanese journal of human genetics最新文献

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A cytogenetic survey on mentally retarded children. 弱智儿童的细胞遗传学调查。
H M Fujita, K Fujita
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引用次数: 0
New Japanese variant of human erythrocyte carbonic anhydrase. 人红细胞碳酸酐酶日本新变种。
N Ueda
{"title":"New Japanese variant of human erythrocyte carbonic anhydrase.","authors":"N Ueda","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 2","pages":"161-7"},"PeriodicalIF":0.0,"publicationDate":"1974-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15326865","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
Probable reciprocal translocation in somatic cells from patients with Down's syndrome. 唐氏综合症患者体细胞中可能存在的相互易位。
S Sonta, H Oishi
{"title":"Probable reciprocal translocation in somatic cells from patients with Down's syndrome.","authors":"S Sonta, H Oishi","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 2","pages":"169-73"},"PeriodicalIF":0.0,"publicationDate":"1974-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15387748","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
Statistical analysis on anencephaly, spina bifida and congenital hydrocephaly in Japan. 日本无脑畸形、脊柱裂和先天性脑积水的统计分析。
Y Imaizumi
{"title":"Statistical analysis on anencephaly, spina bifida and congenital hydrocephaly in Japan.","authors":"Y Imaizumi","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 2","pages":"115-35"},"PeriodicalIF":0.0,"publicationDate":"1974-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15714587","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
[Recurrent Pierre-Robin syndrome in a family with translocation (author's transl)]. [易位家族复发性皮埃尔-罗宾综合征(作者译)]。
K Ohama, H Takahara, I Kuzumi, A Fujiwara
{"title":"[Recurrent Pierre-Robin syndrome in a family with translocation (author's transl)].","authors":"K Ohama, H Takahara, I Kuzumi, A Fujiwara","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 1","pages":"81"},"PeriodicalIF":0.0,"publicationDate":"1974-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15578987","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
[Familial otosclerosis with chromosomal aberration (author's transl)]. 【家族性耳硬化伴染色体畸变(作者译)】。
K Koga, Y Suzuki, M Sakai, M Mukai
{"title":"[Familial otosclerosis with chromosomal aberration (author's transl)].","authors":"K Koga, Y Suzuki, M Sakai, M Mukai","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 1","pages":"85-6"},"PeriodicalIF":0.0,"publicationDate":"1974-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15578994","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
A case of Werner's syndrome. 一个维尔纳综合症的病例。
M Yasuhara, K Kiyokane, T Sakai, T Oiwa, N Hashi
{"title":"A case of Werner's syndrome.","authors":"M Yasuhara, K Kiyokane, T Sakai, T Oiwa, N Hashi","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 1","pages":"86-7"},"PeriodicalIF":0.0,"publicationDate":"1974-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15578995","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
Dermatoglyphics in hypogonadism. 性腺功能减退的皮肤印记。
S Nanko, A Asaka, E Inoue, K Isurugi, K Kinoshita
{"title":"Dermatoglyphics in hypogonadism.","authors":"S Nanko, A Asaka, E Inoue, K Isurugi, K Kinoshita","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":75962,"journal":{"name":"Jinrui idengaku zasshi. The Japanese journal of human genetics","volume":"19 1","pages":"99-100"},"PeriodicalIF":0.0,"publicationDate":"1974-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"15579010","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
Type-dependency in the metabolism of human haptoglobins. II Report. Organ distribution of haptoglobins. 人接触珠蛋白代谢的类型依赖性。二世报告。触珠蛋白的器官分布。
K Kawamura, A Ogawa, H Ohkubo, K Shibata, T Yanase
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引用次数: 0
Polymorphisms of red-cell enzymes and serum proteins (Report 1). 红细胞酶和血清蛋白的多态性(报告1)。
N Ueda, S Kishimoto, H B Hamilton
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引用次数: 0
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