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Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p
A girl fulfilling four/five of six inclusion criteria and eight/nine of 11 supportive criteria for atypical Rett syndrome had a cytogenetic deletion of chromosome 3p, del(3)(pter→3p25.1~25.2). The deletion was situated on the maternally derived chromosome and by molecular analysis the deletion break...
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| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Group
1999
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1734344/ https://ncbi.nlm.nih.gov/pubmed/10227408 |
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