Document Detail

Fine genetic mapping of LCN1/D9S1826 within 9q34.
MedLine Citation:
PMID:  9459006     Owner:  NLM     Status:  MEDLINE    
LCN1 gene encodes the tear lipocalin; the lipocalins are a large and growing family of proteins characterized by their ability to bind small hydrophobic molecules. We report here the location of a dinucleotide repeat microsatellite marker (D9S1826) close to LCN1 gene. Using the CEPH reference families, the position of LCN1 is located within the 9q34 genetic map between D9S23 and D9S158.
E Lacazette; G Pitiot; S Jobert; J Mallet; A M Gachon
Related Documents :
14627806 - Mutagenic stress modulates the dynamics of ctg repeat instability associated with myoto...
8133496 - Mutation size and age at onset in huntington's disease.
8557266 - Molecular re-investigation of patients with huntington's disease in wessex reveals a fa...
8673126 - The molecular basis of hypodactyly (hd): a deletion in hoxa 13 leads to arrest of digit...
8788006 - Use of exact and adjusted liability scores to detect genes affecting common traits.
24212866 - Preparation and flow cytometric analysis of metaphase chromosomes of tomato.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Annals of human genetics     Volume:  61     ISSN:  0003-4800     ISO Abbreviation:  Ann. Hum. Genet.     Publication Date:  1997 Sep 
Date Detail:
Created Date:  1998-03-10     Completed Date:  1998-03-10     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0416661     Medline TA:  Ann Hum Genet     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  449-55     Citation Subset:  IM    
Laboratoire de Biochimie Médicale, Faculté de Médecine, Clermont-Ferrand, France.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Carrier Proteins / genetics*,  isolation & purification
Chromosome Mapping* / methods
Chromosomes, Human, Pair 9 / genetics*
Cosmids / genetics,  isolation & purification
Dinucleotide Repeats / genetics
Lipocalin 1
Microsatellite Repeats / genetics
Polymorphism, Genetic / genetics
Reg. No./Substance:
0/Carrier Proteins; 0/LCN1 protein, human; 0/Lipocalin 1

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Diversity of the human Y chromosome of South American Amerindians: a comparison with blacks, whites,...
Next Document:  Assignment of the human fast skeletal muscle troponin C gene (TNNC2) between D20S721 and GCT10F11 on...