Ellis–van creveld syndrome: A rare autosomal recessive genetic disorder
Ellis–van Creveld syndrome is a rare genetic disorder with autosomal recessive inheritance, mainly affecting the Amish population living in Pennsylvania, USA, with an incidence of 1:244,000 for the general population. This syndrome consists of characteristic features such as bilateral postaxial poly...
محفوظ في:
| المؤلفون الرئيسيون: | , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Wolters Kluwer Medknow Publications
2021-01-01
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| سلاسل: | APIK Journal of Internal Medicine |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.ajim.in/article.asp?issn=2666-1802;year=2021;volume=9;issue=3;spage=180;epage=182;aulast=Ravi |
| الوسوم: |
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