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Clinical presentation of two β-thalassemic Indian patients with 1p36 deletion syndrome: Case report
Here, we present two thalassemic patients (one male and one female), having unusual clinical phenotypes. Both had mental retardation in which one was associated with microcephaly and other had congenital cataract. They were referred to our institute for clinical evaluation and cytogenetic testing. B...
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| Publicat a: | J Pediatr Genet |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Georg Thieme Verlag KG
2014
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5021003/ https://ncbi.nlm.nih.gov/pubmed/27625875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-14097 |
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