[New genetic findings radically improve the diagnostic possibilities in fragile X syndrome]
Lakartidningen
.
1992 Jun 3;89(23):2091-3.
[Article in Swedish]
Authors
N Dahl
1
,
K H Gustavson
,
H Malmgren
,
U Pettersson
Affiliation
1
Avdelningen för klinisk genetik, Akademiska sjukhuset samt institutionen för medicinsk genetik, Biomedicinskt centrum, Uppsala.
PMID:
1630231
No abstract available
Publication types
Review
MeSH terms
DNA / genetics
Female
Fragile X Syndrome / diagnosis
Fragile X Syndrome / genetics*
Genetic Techniques
Humans
Male
Nucleic Acid Hybridization
Pedigree
Substances
DNA