NO EVIDENCE FOR LINKAGE TO THE TYPE-1 OR TYPE-2 NEUROFIBROMATOSIS LOCI IN NOONAN SYNDROME FAMILIES

被引:18
作者
FLINTOFF, WF
BAHUAU, M
LYONNET, S
GILGENKRANTZ, S
LACOMBE, D
MARCON, F
LEVILLIERS, J
KACHANER, J
MUNNICH, A
LEMERRER, M
机构
[1] INSERM,UNITE RECH HANDICAPS GENET ENFANT U12,149 RUE SEVRES,F-75743 PARIS 15,FRANCE
[2] HOP ENFANTS MALAD,SERV CARDIOL,PARIS,FRANCE
[3] INST PASTEUR,UNITE MOLEC HUMAINE,F-75724 PARIS 15,FRANCE
[4] CRTS,GENET LAB,NANCY,FRANCE
[5] CHU BORDEAUX,SERV PEDIAT & GENET,BORDEAUX,FRANCE
[6] CHU NANCY BRABOIS,SERV CARDIOL INFANTILE,NANCY,FRANCE
[7] UNIV WESTERN ONTARIO,DEPT MICROBIOL & IMMUNOL,LONDON N6A 3K7,ONTARIO,CANADA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 46卷 / 06期
关键词
NF1; NF2; LINKAGE; CHROMOSOME; 17Q; 22Q;
D O I
10.1002/ajmg.1320460621
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A linkage analysis has been performed on 6 two-generation families with classical Noonan syndrome to determine whether the syndrome is linked to neurofibromatosis type 1 on chromosome 17q or to neurofibromatosis type 2 on chromosome 22q. A significantly negative location score was obtained between 10 cM centromeric to and 15 cM telomeric from the neurofibromatosis type 1 locus. A significantly negative lod score was obtained with a marker mapping within the region where neurofibromatosis type 2 is thought to be located. These data indicate that Noonan syndrome is not tightly linked to either neurofibromatosis type 1 or type 2. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:700 / 705
页数:6
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