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


Autoria(s): Zoll B.; Arnemann J.; Krawczak M.; Cooper D.N.; Pescia G.; Wahli W.; Steinbach P.; Schmidtke J.
Data(s)

1985

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_8A5E20773819

isbn:0340-6717[print], 0340-6717[linking]

pmid:2995232

isiid:A1985ASF0800007

Idioma(s)

en

Fonte

Human Genetics, vol. 71, no. 2, pp. 122-126

Palavras-Chave #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
Tipo

info:eu-repo/semantics/article

article