ISI Web of Knowledge Take the next step  
Web of Science®
 
Previous Record (inactive) Record 1  of  1 Next Record (inactive)
Record from Web of Science®
NO EVIDENCE FOR LINKAGE TO THE TYPE-1 OR TYPE-2 NEUROFIBROMATOSIS LOCI IN NOONAN SYNDROME FAMILIES
Author(s): FLINTOFF WF, BAHUAU M, LYONNET S, GILGENKRANTZ S, LACOMBE D, MARCON F, LEVILLIERS J, KACHANER J, MUNNICH A, LEMERRER M
Source: AMERICAN JOURNAL OF MEDICAL GENETICS    Volume: 46    Issue: 6    Pages: 700-705    Published: JUL 1 1993  
Times Cited: 16     References: 30     
Abstract: 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.
Document Type: Article
Language: English
Addresses:
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
Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC 605 THIRD AVE, NEW YORK, NY 10158-0012
Subject Category: Genetics & Heredity
IDS Number: LP905
ISSN: 0148-7299
Previous Record (inactive) Record 1  of  1 Next Record (inactive)
Record from Web of Science®
  
Thomson Reuters Logo