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新发9号染色体异常患儿的临床和细胞遗传学研究
This study aimed to analyze the clinical phenotype of chromosome 9p deletion or duplication and its relationship with karyotype. A patient, female, aged 6 months, visited the hospital due to motor developmental delay. Karyotype analysis identified abnormalities of chromosome 9 short arm, and high-th...
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| Yayımlandı: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
中国当代儿科杂志编辑部
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7390313/ https://ncbi.nlm.nih.gov/pubmed/29335083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2018.01.011 |
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