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Development of rib-vertebrae: a new mutation in the house mouse with accessory caudal duplications.

作者信息

Theiler K, Varnum D S

出版信息

Anat Embryol (Berl). 1985;173(1):111-6. doi: 10.1007/BF00707309.

DOI:10.1007/BF00707309
PMID:4073528
Abstract

The new recessive mutation rib-vertebrae (rv) causes fusions of lower ribs and malformations of vertebrae, which results from disturbed somite arrangement. In addition, duplications of the caudal neural tube and sometimes unilateral suppression of kidney formation can be observed. The new mutation is compared with the six already known mutations in mice with "Wirbel-Rippen-Syndrome" and with a similar syndrome in man. From the various effects of the rv-gene observed, it is suggested that the gene causes abnormal inner and outer surface formation, producing manifold secondary effects.

摘要

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本文引用的文献

1
Anatomy and development of the "truncate" (boneless) mutation in the mouse.小鼠“截短”(无骨)突变的解剖结构与发育
Am J Anat. 1959 May;104:319-43. doi: 10.1002/aja.1001040302.
2
The development of rib fusions, a mutation in the house mouse.肋骨融合的发育,家鼠中的一种突变。
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3
The morphological effects and the development of the fused mutation in the mouse.小鼠中融合突变的形态学效应及发展
一项关于猪脊椎数量的研究证实了vertnin的关联,并揭示了其他数量性状基因座。
BMC Genet. 2015 Oct 30;16:129. doi: 10.1186/s12863-015-0286-9.
4
TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia.TBX6、LHX1 和 Müllerian 发育不全的复杂遗传学中的拷贝数变异。
Orphanet J Rare Dis. 2013 Aug 16;8:125. doi: 10.1186/1750-1172-8-125.
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[Costovertebral dysplasia. A receptor defect of sclerotome development?].
Schweiz Med Wochenschr. 1982 May 29;112(22):791-7.
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[Vertebra-rib syndrome].
Schweiz Med Wochenschr. 1968 Jun 15;98(24):907-8.
6
Development of rachiterata, a mutation in the house mouse with 6 cervical vertebrae.佝偻病小鼠的发育,家鼠中一种具有6块颈椎骨的突变。
Z Anat Entwicklungsgesch. 1974;145(1):75-80. doi: 10.1007/BF00519127.
7
Malformed vertebrae: a new mutant with the "wirbel-rippen syndrom" in the mouse.畸形椎骨:小鼠中一种具有“脊椎-肋骨综合征”的新突变体。
Anat Embryol (Berl). 1975 Aug 9;147(2):161-6. doi: 10.1007/BF00306730.