ロード中...
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 |
|---|---|
| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
1990
|
| 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|