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Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.
X inactivation studies have been carried out on lymphocytes from eight unrelated females heterozygous for the Martin-Bell syndrome. Four of these carriers were of normal IQ and four were mentally handicapped. When BrdU was used to differentiate between the active and inactive X chromosome an average...
保存先:
| 出版年: | J Med Genet |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
1990
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017241/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2246771/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.10.627 |
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