Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)

American Journal of Human Genetics

Volumn 48, Issue 1, 1991, Pages 108-116

  Rousseau, F ^a   Vincent, A ^a   Rivella, S ^a   Heitz, D ^a   Triboli, C ^a   Maestrini, E ^a   Warren, S T ^a   Suthers, G K ^a   Goodfellow, P ^a   Mandel, J L ^a   Toniolo, D ^a   Oberle, I ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME BREAKAGE; CHROMOSOME XQ; DNA PROBE; FRAGILE X SYNDROME; GENE LOCUS; GENE MAPPING; HUMAN; HUMAN CELL; HYBRID CELL; PRIORITY JOURNAL;

BLOTTING, SOUTHERN; DNA PROBES; FRAGILE X SYNDROME; GENETIC MARKERS; HUMAN; LINKAGE (GENETICS); POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RESTRICTION MAPPING; SUPPORT, NON-U.S. GOV'T;

EID: 0026068620     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)