Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX.

Détails

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ID Serval
serval:BIB_8A5E20773819
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
UNIL/CHUV
Titre
Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX.
Périodique
Human Genetics
Auteur⸱e⸱s
Zoll B., Arnemann J., Krawczak M., Cooper D.N., Pescia G., Wahli W., Steinbach P., Schmidtke J.
ISSN
0340-6717[print], 0340-6717[linking]
Statut éditorial
Publié
Date de publication
1985
Volume
71
Numéro
2
Pages
122-126
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Linkage between the loci for fraXq of Martin-Bell syndrome and factor IX was studied in nine families exhibiting this syndrome by means of a restriction fragment length polymorphism at the factor IX locus. Computer analysis of the data indicates there to be no evidence for close linkage between the syndrome and the factor IX locus.
Mots-clé
Chromosome Fragility, Chromosome Mapping, DNA Restriction Enzymes, Deoxyribonucleases, Type II Site-Specific, Electrophoresis, Agar Gel, Factor IX/genetics, Female, Genetic Markers, Humans, Linkage (Genetics), Male, Mental Retardation/genetics, Pedigree, Syndrome, X Chromosome
OAI-PMH
oai:serval.unil.ch:BIB_8A5E20773819
Pubmed
2995232
Web of science
A1985ASF0800007
Création de la notice
24/01/2008 17:04
Dernière modification de la notice
20/08/2019 15:49
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