Face facts: genes, environment, and clefts.
作者信息
Murray J C
出版信息
Am J Hum Genet. 1995 Aug;57(2):227-32.
Abstract
摘要
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本文引用的文献
1
A region of the mouse genome homologous to human chromosome 1q21 affects facial clefting.小鼠基因组中与人类1号染色体1q21区域同源的部分会影响面部裂隙。
J Craniofac Genet Dev Biol. 1993 Jan-Mar;13(1):1-5.
2
TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice.转化生长因子α缺乏会导致靶向小鼠和waved-1小鼠出现毛囊和眼睛异常。
Cell. 1993 Apr 23;73(2):263-78. doi: 10.1016/0092-8674(93)90228-i.
3
Vitamin A-enhanced cleft palate susceptibility gene maps between C4 and B144 within the H-2 complex.维生素A增强型腭裂易感性基因定位于H-2复合体中C4和B144之间。
Proc Soc Exp Biol Med. 1993 Apr;202(4):482-6. doi: 10.3181/00379727-202-43563.
4
Inhibition of neural crest cell attachment by integrin antisense oligonucleotides.整合素反义寡核苷酸对神经嵴细胞黏附的抑制作用。
Science. 1993 Jan 29;259(5095):692-5. doi: 10.1126/science.8430321.
5
Exclusion of candidate genes from a role in cleft lip with or without cleft palate: linkage and association studies.排除候选基因在伴或不伴腭裂的唇裂发病中的作用：连锁与关联研究
J Med Genet. 1993 Sep;30(9):773-8. doi: 10.1136/jmg.30.9.773.
6
High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice.视黄酸受体α突变小鼠的高出生后致死率和睾丸退化
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7225-9. doi: 10.1073/pnas.90.15.7225.
7
A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus.在小鼠p位点的一个神经学突变体中，一组三个GABAA受体亚基基因被删除。
Nature. 1993 Jul 29;364(6436):448-50. doi: 10.1038/364448a0.
8
Linkage analysis versus association analysis: distinguishing between two models that explain disease-marker associations.连锁分析与关联分析：区分两种解释疾病-标记物关联的模型。
Am J Hum Genet. 1993 Aug;53(2):367-84.
9
10
Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1.内皮素-1缺乏小鼠的血压升高和颅面异常
Nature. 1994 Apr 21;368(6473):703-10. doi: 10.1038/368703a0.
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