A case report of Monosomy 21
monosomy 21 is a rare chromosomal abnormality which is persented in mosaic or homogenous forms.the latter form which is very rare,is determined by intra uterin growth retardation)IUGR),failure to thrive (FTT),prominent craniofacial,skeletal deformities and differnt degrees of delay in psychomotor ac...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Kerman University of Medical Sciences
1999-03-01
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| Seri Bilgileri: | Journal of Kerman University of Medical Sciences |
| Konular: | |
| Online Erişim: | https://jkmu.kmu.ac.ir/article_34286_9b13194d1ab6dc38090cc3b48bed2386.pdf |
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