Linkage studies in peripheral neurofibromatosis.
Linkage studies in peripheral neurofibromatosis.
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周围神经纤维瘤病的关联研究。
DOI:
10.1136/jmg.24.9.530
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发表时间:
1987
影响因子:
4
通讯作者:
Roses,AD
中科院分区:
文献类型:
--
作者:
Pericak-Vance,MA;Yamaoka,LH;Vance,JM;Aylsworth,AS;Rossenwasser,GO;GaskellJr,PC;Alberts,MJ;Hung,WY;Haynes,C;Roses,AD
Peripheral neurofibromatosis (NF) is one of the most common major genetic disorders in man. Its chromosomal location is unknown and questions regarding such factors as genetic heterogeneity remain unanswered. We have ascertained and sampled several large multi-generation families for linkage studies including one family of 66 subjects, 28 of whom were affected with NF. Recombinant DNA studies of several restriction fragment length polymorphisms (RFLPs) including C3, ApoC2, pBam34 (D19S6], HAUP[APRT], pE40-1 [D11521], Hp[Hp2 alpha], LDR92, and LDR111 failed to show a significant linkage (Z [lod score] greater than or equal to 3.00) in this family. In addition, the results excluded areas of the genome around the marker loci (Z greater than or equal to - 2.00) as potential sites for linkage. The maximum Z obtained with the markers was for Hp at theta (maximum recombination fraction) = 0.20 and Z = 0.399. We are now in the process of screening additional RFLPs and families for linkage to NF.
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影响因子:
17.3
作者:
R. I. S. Bayliss
通讯作者:
R. I. S. Bayliss
DOI:
--
发表时间:
1979
期刊:
Birth defects original article series
影响因子:
--
作者:
John C. Carey;Laub Jm;Bryan D. Hall
通讯作者:
Bryan D. Hall
DOI:
10.1159/000132011
发表时间:
1982
期刊:
Birth defects original article series
影响因子:
--
作者:
H. Willard;M. Skolnick;P. Pearson;J. Mandel
通讯作者:
J. Mandel
影响因子:
4
作者:
Spence,MA;Bader,JL;Parry,DM;Field,LL;Funderburk,SJ;Rubenstein,AE;Gilman,PA;Sparkes,RS
通讯作者:
Sparkes,RS