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Journal of mental deficiency research最新文献

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Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation). 氏综合症。(张力减退、肥胖、性腺功能减退、生长发育和智力低下)。
Journal of mental deficiency research Pub Date : 2010-07-22 DOI: 10.1111/J.1365-2788.1971.TB01137.X
J. Jancar
{"title":"Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation).","authors":"J. Jancar","doi":"10.1111/J.1365-2788.1971.TB01137.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1971.TB01137.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"15 1 1","pages":"20-9"},"PeriodicalIF":0.0,"publicationDate":"2010-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1971.TB01137.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63030766","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: 35
"Rubinstein-Taybi's syndrome". “Rubinstein-Taybi综合征”。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1965.TB00845.X
J. Jancar
{"title":"\"Rubinstein-Taybi's syndrome\".","authors":"J. Jancar","doi":"10.1111/J.1365-2788.1965.TB00845.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1965.TB00845.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"9 4 1","pages":"265-70"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1965.TB00845.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63029384","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: 16
Cue salience and learning in severely sub-normal children. Effects of varying the attention value of the cues employed in a one-trial learning situation. 提示严重亚正常儿童的显著性和学习能力。单次学习情境中不同提示注意值的影响。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1972.TB01582.X
J. Sinson, N. Wetherick
{"title":"Cue salience and learning in severely sub-normal children. Effects of varying the attention value of the cues employed in a one-trial learning situation.","authors":"J. Sinson, N. Wetherick","doi":"10.1111/J.1365-2788.1972.TB01582.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1972.TB01582.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"16 2 1","pages":"112-8"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1972.TB01582.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63031222","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: 5
Children with supernumerary X-chromosome. A ten-year follow-up study of schoolchildren in special classes. 有多余x染色体的儿童。一项针对特殊班级学生的十年跟踪研究。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1979.TB00994.X
H. Forssman, I. Thuwe, B. Eriksson
{"title":"Children with supernumerary X-chromosome. A ten-year follow-up study of schoolchildren in special classes.","authors":"H. Forssman, I. Thuwe, B. Eriksson","doi":"10.1111/J.1365-2788.1979.TB00994.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1979.TB00994.X","url":null,"abstract":"Pupils from special school classes affected by supernumerary X-chromosomes (eight girls and eighteen boys) were subjected to a follow-up study over a period of ten years. The risks of social behaviour disturbances, criminality and alcohol abuse were studied, together with that of mental disorder. In the case of the girls no statistically significant differences were found. For the boys, the only difference of statistical significance was that the Klinefelter boys showed a lower frequency of social behaviour disturbances that their controls.","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"23 3 1","pages":"189-93"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1979.TB00994.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63031525","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
Penylketonuria detection of the heterozygous carrier. 杂合载体戊基酮尿的检测。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1957.TB00280.X
D. Hsia, R. Paine
{"title":"Penylketonuria detection of the heterozygous carrier.","authors":"D. Hsia, R. Paine","doi":"10.1111/J.1365-2788.1957.TB00280.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1957.TB00280.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"1 1 1","pages":"53-65"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1957.TB00280.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63027202","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: 22
Potter's syndrome with mental retardation (auro-renal syndrome; reno-facial dysplasia). 波特综合征伴智力迟钝(光肾综合征);reno-facial发育不良)。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1969.TB01061.X
J. Jancar
{"title":"Potter's syndrome with mental retardation (auro-renal syndrome; reno-facial dysplasia).","authors":"J. Jancar","doi":"10.1111/J.1365-2788.1969.TB01061.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1969.TB01061.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"13 1 1","pages":"8-12"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1969.TB01061.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63030361","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: 5
A cytogenetic study of 77 Chinese children with Down's syndrom. 77例中国唐氏综合征患儿的细胞遗传学研究。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1967.TB00216.X
S. W. Huang, I. Emanuel, J. Lo, S. Liao, C. Hsu
{"title":"A cytogenetic study of 77 Chinese children with Down's syndrom.","authors":"S. W. Huang, I. Emanuel, J. Lo, S. Liao, C. Hsu","doi":"10.1111/J.1365-2788.1967.TB00216.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1967.TB00216.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"11 3 1","pages":"147-52"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1967.TB00216.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63030321","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: 18
Monosomy G mosaicism in twonrelated children. 两个相关儿童的单体G镶嵌现象。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1968.TB00266.X
J. Schulz, E. Krmpotic
{"title":"Monosomy G mosaicism in twonrelated children.","authors":"J. Schulz, E. Krmpotic","doi":"10.1111/J.1365-2788.1968.TB00266.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1968.TB00266.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"12 4 1","pages":"255-67"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1968.TB00266.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63030671","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: 10
Dementia infantilis Heller; diagnostic problems with a case report. 婴儿痴呆;用病例报告诊断问题。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1957.TB00002.X
V. Hudolin
{"title":"Dementia infantilis Heller; diagnostic problems with a case report.","authors":"V. Hudolin","doi":"10.1111/J.1365-2788.1957.TB00002.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1957.TB00002.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"15 1","pages":"79-90"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1957.TB00002.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63027117","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: 20
An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree. 易位(Cq-，Aq+)家系中的不平衡核型。
Journal of mental deficiency research Pub Date : 2008-06-28 DOI: 10.1111/J.1365-2788.1969.TB01072.X
G. F. Smith, C. Shear, I. Jalowayski, H. Åkesson
{"title":"An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.","authors":"G. F. Smith, C. Shear, I. Jalowayski, H. Åkesson","doi":"10.1111/J.1365-2788.1969.TB01072.X","DOIUrl":"https://doi.org/10.1111/J.1365-2788.1969.TB01072.X","url":null,"abstract":"","PeriodicalId":76014,"journal":{"name":"Journal of mental deficiency research","volume":"13 2 1","pages":"123-9"},"PeriodicalIF":0.0,"publicationDate":"2008-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/J.1365-2788.1969.TB01072.X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"63030495","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: 5
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