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Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene.

作者信息

Pasteris N G, de Gouyon B, Cadle A B, Campbell K, Herman G E, Gorski J L

机构信息

Department of Human Genetics, University of Michigan Medical Center, Ann Arbor 48109-0688, USA.

出版信息

Mamm Genome. 1995 Sep;6(9):658-61. doi: 10.1007/BF00352375.

DOI:10.1007/BF00352375
PMID:8535076
Abstract
摘要

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Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene.
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Mol Cell Biol. 2011 Nov;31(22):4430-41. doi: 10.1128/MCB.05474-11. Epub 2011 Sep 12.
2
Comparative genome organization of vertebrates. The First International Workshop on Comparative Genome Organization.脊椎动物的比较基因组组织。第一届比较基因组组织国际研讨会。
Mamm Genome. 1996 Oct;7(10):717-34. doi: 10.1007/s003359900222.
3
Smcx lies distal to DXHX674 and DXHX679 on the mouse X chromosome.

本文引用的文献

1
Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.
Mamm Genome. 1993;4(3):171-6. doi: 10.1007/BF00352233.
2
Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323.
Hum Mol Genet. 1993 Oct;2(10):1717-8. doi: 10.1093/hmg/2.10.1717.
3
Proteins regulating Ras and its relatives.调节Ras及其相关蛋白。
Nature. 1993 Dec 16;366(6456):643-54. doi: 10.1038/366643a0.
4
Mamm Genome. 1996 Jul;7(7):552. doi: 10.1007/s003359900286.
New insights into the man-mouse comparative map of the X chromosome.X染色体人鼠比较图谱的新见解。
Genomics. 1994 Jan 15;19(2):212-20. doi: 10.1006/geno.1994.1050.
5
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor.面生殖器发育异常（阿斯克格-斯科特综合征）基因的分离与鉴定：一种假定的Rho/Rac鸟嘌呤核苷酸交换因子
Cell. 1994 Nov 18;79(4):669-78. doi: 10.1016/0092-8674(94)90552-5.
6
Genetic linkage of the erythroid-specific delta-aminolevulinate synthase gene (Alas2) to the distal region of the mouse X chromosome.红细胞特异性δ-氨基乙酰丙酸合酶基因（Alas2）与小鼠X染色体远端区域的遗传连锁。
Mamm Genome. 1994 Nov;5(11):741. doi: 10.1007/BF00426087.
7
Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome.
Am J Med Genet. 1994 Sep 1;52(3):339-45. doi: 10.1002/ajmg.1320520317.
8
Mouse X chromosome.
Mamm Genome. 1994;5 Spec No:S276-88.
9
Aarskog syndrome: full male and female expression associated with an X-autosome translocation.
Am J Med Genet. 1984 Mar;17(3):595-602. doi: 10.1002/ajmg.1320170307.
10
A comprehensive set of sequence analysis programs for the VAX.一套适用于VAX的综合序列分析程序。
Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387-95. doi: 10.1093/nar/12.1part1.387.