The Journal of clinical dysmorphology最新文献

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Proteus syndrome. 普罗透斯综合症。
R J Gorlin
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引用次数: 0
A photographic study: the natural history of Prader-Willi syndrome. 摄影研究:普瑞德-威利综合征的自然历史。
F Char
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引用次数: 0
Sensorineural hearing loss, small facial features, submucous cleft palate, and myoclonic seizures. 感音神经性听力损失,小面部特征,粘膜下腭裂和肌阵挛性癫痫。
M Preus, A R Cooper, E O'Leary
{"title":"Sensorineural hearing loss, small facial features, submucous cleft palate, and myoclonic seizures.","authors":"M Preus, A R Cooper, E O'Leary","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"2 1","pages":"30-1"},"PeriodicalIF":0.0,"publicationDate":"1984-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17642782","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
The Proteus Syndrome: the emergence of an entity. 普罗透斯综合症:一个实体的出现。
D B Lezama, M L Buyse
{"title":"The Proteus Syndrome: the emergence of an entity.","authors":"D B Lezama, M L Buyse","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"2 1","pages":"10-3"},"PeriodicalIF":0.0,"publicationDate":"1984-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17485517","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
Mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasia. 中度侏儒症,骨骼异常,外胚层发育不良。
D Brunoni
{"title":"Mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasia.","authors":"D Brunoni","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"2 1","pages":"14-8"},"PeriodicalIF":0.0,"publicationDate":"1984-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17642778","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
Short-limbed dwarfism, subluxation of the knees, hypogenitalism, and dysmorphic facies: a new syndrome? 短肢侏儒症、膝关节半脱位、性器官减退和畸形相:一种新的综合征?
P J Willems, S De Vries-Van der Weerd, F J Los, J M Mandema, G P Smit
{"title":"Short-limbed dwarfism, subluxation of the knees, hypogenitalism, and dysmorphic facies: a new syndrome?","authors":"P J Willems, S De Vries-Van der Weerd, F J Los, J M Mandema, G P Smit","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"2 1","pages":"19-21"},"PeriodicalIF":0.0,"publicationDate":"1984-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17642779","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
Autosomal dominant blepharophimosis with multiple congenital anomalies. 常染色体显性眼睑病伴多重先天性异常。
B F Krieble, D Bixler
{"title":"Autosomal dominant blepharophimosis with multiple congenital anomalies.","authors":"B F Krieble, D Bixler","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"2 1","pages":"24-9"},"PeriodicalIF":0.0,"publicationDate":"1984-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17642781","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
Pigmentary characteristics of the ectodermal dysplasias. 外胚层发育不良的色素特征。
B R Elejalde, M M de Elejalde
{"title":"Pigmentary characteristics of the ectodermal dysplasias.","authors":"B R Elejalde, M M de Elejalde","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"1 1","pages":"2-8"},"PeriodicalIF":0.0,"publicationDate":"1983-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17635950","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
Syndrome identification case report 96: syngnathia and multiple defects. 综合征鉴定病例报告96例:合颌伴多重缺陷。
B Dobrow
{"title":"Syndrome identification case report 96: syngnathia and multiple defects.","authors":"B Dobrow","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"1 2","pages":"5-7"},"PeriodicalIF":0.0,"publicationDate":"1983-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17635962","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
Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies. 发育迟缓,生长缺陷,先天性心脏缺陷,多发性颅面异常。
I Rommen, R F Mueller, V P Sybert
{"title":"Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies.","authors":"I Rommen, R F Mueller, V P Sybert","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":79272,"journal":{"name":"The Journal of clinical dysmorphology","volume":"1 4","pages":"10-3"},"PeriodicalIF":0.0,"publicationDate":"1983-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"17648140","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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