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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1983 | 1 |
1984 | 1 |
2024 | 0 |
Search Results
2 results
Results by year
Filters applied: . Clear all
Page 1
Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.
Hum Genet. 1983;64(4):388-94. doi: 10.1007/BF00292373.
Hum Genet. 1983.
PMID: 6618490
Duplication or insertion in 15q11-13 associated with mental retardation-short stature and obesity-Prader-Willi or Cohen syndrome?
Fuhrmann-Rieger A, Köhler A, Fuhrmann W.
Fuhrmann-Rieger A, et al.
Clin Genet. 1984 Apr;25(4):347-52. doi: 10.1111/j.1399-0004.1984.tb02002.x.
Clin Genet. 1984.
PMID: 6713711
Item in Clipboard
Cite
Cite