טוען...
X linked alpha thalassaemia/mental retardation: spectrum of clinical features in three related males.
We describe three males (two brothers and a cousin) who have the X linked alpha thalassaemia/mental retardation (ATR-X) syndrome. The diagnosis, originally suspected in the brothers because of similarity in dysmorphic features to previous cases, was confirmed haematologically in the surviving brothe...
שמור ב:
| הוצא לאור ב: | J Med Genet |
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| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
1991
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017107/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1770529/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.11.738 |
| תגים: |
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