Linkage analysis of candidate endothelin pathway genes in nonsyndromic familial orofacial cleft

被引:11
|
作者
Pezzetti, F
Scapoli, L
Martinelli, M
Carinci, F
Brunelli, G
Carls, FP
Palomba, F
Gombos, F
Carinci, P
Tognon, M
机构
[1] Univ Ferrara, Dept Morphol & Embryol, Sect Histol & Embryol, I-44100 Ferrara, Italy
[2] Univ Ferrara, Ctr Biotechnol, I-44100 Ferrara, Italy
[3] Univ Ferrara, Chair Maxillofacial Surg, I-44100 Ferrara, Italy
[4] John Radcliffe Hosp, Dept Maxillofacial Surg, Oxford OX3 9DU, England
[5] SUN, Odontoiatr Clin 1, I-80100 Naples, Italy
[6] Univ Bologna, Inst Histol & Gen Embryol, I-40126 Bologna, Italy
关键词
D O I
10.1046/j.1469-1809.2000.6440341.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There is good evidence from linkage analysis and mouse model knockouts that the endothelin-1 gene (EDN1) is a good candidate for non-syndromic orofacial cleft (OFC) disease. EDN1 maps to the chromosomal region of the OFC1 locus in 6p23. Therefore we have examined three other candidate genes in the endothelin pathway (ECE1, EDNRA and EDNRB, which map to chromosomes 1, 4 and 13 respectively) in a linkage study of 9 families with OFC, where the disorder is not linked to chromosome 6p23. The total lod score for these 9 multiplex families never exceeded -2.00 and thus our data suggest that EDN1 and related genes are not involved in non-syndromic familial CEC.
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页码:341 / 347
页数:7
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