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对意大利一组连续性唇裂伴或不伴腭裂新生儿样本进行复杂分离分析。

Complex segregation analysis in a sample of consecutive newborns with cleft lip with or without cleft palate in Italy.

作者信息

Clementi M, Tenconi R, Collins A, Calzolari E, Milan M

机构信息

Dipartimento di Pediatria, Università di Padova, Italia.

出版信息

Hum Hered. 1995 May-Jun;45(3):157-64. doi: 10.1159/000154277.

Abstract

The mode of inheritance of cleft lip with or without cleft palate (CL/P) has been extensively investigated, but the results are controversial. We report results of complex segregation analysis performed in the families of 636 consecutive newborns with CL/P registered in the northeast Italy and Emilia Romagna congenital malformation registries to test hypotheses regarding CL/P inheritance. The programs POINTER and COMDS have been used. POINTER could not distinguish between alternative genetic models, and only the hypothesis of no familial transmission could be rejected. COMDS results, after inclusion of the severity parameter, rejected the hypotheses of a single major locus and were consistent with the two-locus model with a major dominant locus and at least one modifier locus.

摘要

唇裂伴或不伴腭裂(CL/P)的遗传模式已得到广泛研究,但结果存在争议。我们报告了对意大利东北部和艾米利亚-罗马涅先天性畸形登记处登记的636例连续新生儿CL/P家族进行的复杂分离分析结果,以检验有关CL/P遗传的假设。使用了POINTER和COMDS程序。POINTER无法区分替代遗传模型,仅无家族遗传的假设可以被拒绝。纳入严重程度参数后的COMDS结果拒绝了单一主基因座的假设,与具有一个主要显性基因座和至少一个修饰基因座的双基因座模型一致。

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