Датотека:Partial Deletion of Short Arms of 5.jpg
Величина овог приказа: 745 × 600 пиксела. 6 других резолуција: 298 × 240 пиксела | 596 × 480 пиксела | 954 × 768 пиксела | 1.272 × 1.024 пиксела | 2.543 × 2.048 пиксела | 3.139 × 2.528 пиксела.
Оригинална датотека (3.139 × 2.528 пиксела, величина датотеке: 296 kB, MIME тип: image/jpeg)
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Опис
| Опис |
English: This photographic collage depicts the karyotype that would represent the chromosomal configuration known as an autosomal deletion syndrome, which has been given the name, cri-du-chat. In this particular case, the cells in a person with cri-du-chat syndrome contained an abnormal chromosomal complement, which involved the deletion of some of the chromosomal material from the short arms of chromosome 5 (5p-), as indicated by the arrow. Cri-du-chat syndrome was the first recognized syndrome due to a chromosomal deletion, in 1963. Aspects of the syndrome manifest themselves as mental retardation, microcephaly, round face, and a laryngeal anomaly that causes infants to sound like a cat when crying, hence its moniker. |
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| Извор | https://phil.cdc.gov/Details.aspx?pid=12505 |
| Аутор | CDC/ Dr. Allan Ebbin |
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This media comes from the Centers for Disease Control and Prevention's Public Health Image Library (PHIL), with identification number #12505. Note: Not all PHIL images are public domain; be sure to check copyright status and credit authors and content providers.
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Лиценцирање
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This image is a work of the Centers for Disease Control and Prevention, part of the United States Department of Health and Human Services, taken or made as part of an employee's official duties. As a work of the U.S. federal government, the image is in the public domain.
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| Датум/време | Минијатура | Димензије | Корисник | Коментар | |
|---|---|---|---|---|---|
| тренутна | 19:23, 14. септембар 2020. | | 3.139 × 2.528 (296 kB) | AntiCompositeNumber | {{Information |description ={{en|1=This photographic collage depicts the karyotype that would represent the chromosomal configuration known as an autosomal deletion syndrome, which has been given the name, cri-du-chat. In this particular case, the cells in a person with cri-du-chat syndrome contained an abnormal chromosomal complement, which involved the deletion of some of the chromosomal material from the short arms of chromosome 5 (5p-), as indicated by the arrow. Cri-du-chat syndrome wa... |
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