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Titlebook: Gene Regulatory Sequences and Human Disease; Nadav Ahituv Book 2012 Springer Science+Business Media, LLC 2012 Systems Biology

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發(fā)表于 2025-3-26 23:45:40 | 只看該作者
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發(fā)表于 2025-3-27 02:20:39 | 只看該作者
Verwaltungskultur im Ausl?nderamtof fragility fracture. Genetic factors play an important role in regulating bone mineral density (BMD) and other phenotypes relevant to the pathogenesis of osteoporosis. It is currently believed that a large number of susceptibility alleles contribute to the risk of osteoporosis each with a small ef
33#
發(fā)表于 2025-3-27 07:13:21 | 只看該作者
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發(fā)表于 2025-3-27 11:12:49 | 只看該作者
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發(fā)表于 2025-3-27 15:08:46 | 只看該作者
,Interkulturalit?t: Terminologische Aspekte,cted individual, their families, and society provides strong motivation to understand the causes. Initial genetic studies focused on coding regions of genes that are required for normal development of the lip and palate. However, many individuals with cleft lip and palate do not have mutations in th
36#
發(fā)表于 2025-3-27 19:35:20 | 只看該作者
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發(fā)表于 2025-3-28 00:37:27 | 只看該作者
Forschung Erziehungswissenschaftrldwide (WHO 2010). The etiology of hearing loss is varied and can include environmental noise, physical trauma to the head, infections, ototoxic compounds, and the natural aging process. Heritable hearing loss segregating as a Mendelian trait is thought to constitute but a fraction of cases; noneth
38#
發(fā)表于 2025-3-28 04:16:19 | 只看該作者
,Lehren für eine bunte Republik?,he absence of variable length of the submucous (Meissner’s) and myenteric (Auerbach’s) plexuses in the distal gut. As a defect in neural crest-derived cell population, Hirschsprung disease is considered a neurocristopathy. While HSCR was originally observed in sporadic cases, the advent of lifesavin
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發(fā)表于 2025-3-28 07:13:43 | 只看該作者
40#
發(fā)表于 2025-3-28 12:46:17 | 只看該作者
Ich habe meinen Anwalt bei mir …ys essential cellular functions in sister chromatid cohesion during mitosis and meiosis, DNA repair, gene expression, and maintaining 3-D genome organization. Cohesin is required for cell division, maintaining pluripotency of stem cells and ensuring normal organ development. Defective cohesin genes
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