Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
J Med Genet. 1986 Dec;23(6):573-80. doi: 10.1136/jmg.23.6.573.
J Med Genet. 1986.
PMID: 2879929
Free PMC article.
Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 region.
Skraastad MI, Bakker E, de Lange LF, Vegter-van der Vlis M, Klein-Breteler EG, van Ommen GJ, Pearson PL.
Skraastad MI, et al. Among authors: de lange lf.
Am J Hum Genet. 1989 Apr;44(4):560-6.
Am J Hum Genet. 1989.
PMID: 2564732
Free PMC article.
Item in Clipboard
Duchenne muscular dystrophy in females: a rare genetic disorder and occupational therapy perspectives.
Schroeder-Smith K, Tischenkel C, Delange L, Lou JQ.
Schroeder-Smith K, et al.
Occup Ther Health Care. 2002;14(2):79-96. doi: 10.1080/J003v14n02_06.
Occup Ther Health Care. 2002.
PMID: 23930587
Item in Clipboard
Cite
Cite