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A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42
We report a case of partial deletion of 9p with partial trisomy of 1q42 syndrome, which is a rare clinical and cytogenetic report. The dysmorphic features of the patient include microcephaly, plagiocephaly, trigonocephaly with metopic ridge, arched eyebrows, hypertelorism, down-slanting palpebral fi...
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| Publicat a: | Maedica (Bucur) |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
EDITORIAL POINT OF VIEW
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5574076/ https://ncbi.nlm.nih.gov/pubmed/28878839 |
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