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 |
---|---|
1977 | 1 |
1987 | 1 |
1995 | 1 |
2001 | 1 |
2024 | 0 |
Search Results
4 results
Results by year
Filters applied: . Clear all
Page 1
Fanconi anemia, dyskeratosis congenita, and WT syndrome.
Am J Med Genet Suppl. 1987;3:263-78. doi: 10.1002/ajmg.1320280531.
Am J Med Genet Suppl. 1987.
PMID: 2453204
Review.
As a result, other similar conditions, such as dyskeratosis congenita and particularly WT syndrome, are often mistaken for Fanconi anemia. However, at a closer look, the type of congenital anomalies, the mode of inheritance, cytogenic and other laboratory findings a …
As a result, other similar conditions, such as dyskeratosis congenita and particularly WT syndrome, are often mistaken for Fan …
[WT syndrome].
Nakamura M.
Nakamura M.
Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):823.
Ryoikibetsu Shokogun Shirizu. 2001.
PMID: 11529042
Review.
Japanese.
No abstract available.
Item in Clipboard
A patient with WT syndrome and Castleman disease.
Vergin C, Cetingül N, Kavakli K, Oztop S, Ozkinay F, Coker M, Nişli G, Soydan S, Balik E, Akar O.
Vergin C, et al.
Acta Paediatr Jpn. 1995 Feb;37(1):108-12. doi: 10.1111/j.1442-200x.1995.tb03700.x.
Acta Paediatr Jpn. 1995.
PMID: 7754753
WT syndrome, an autosomal dominant condition, combines hematological abnormalities with mild lib defects. ...This interesting patient is reported because Castleman disease, together with WT syndrome has not been previously described....
WT syndrome, an autosomal dominant condition, combines hematological abnormalities with mild lib defects. ...This interesting …
Item in Clipboard
The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia.
Gonzalez CH, Durkin-Stamm MV, Geimer NF, Shahidi NT, Schilling RF, Rubira F, Opitz JM.
Gonzalez CH, et al.
Birth Defects Orig Artic Ser. 1977;13(3B):31-8.
Birth Defects Orig Artic Ser. 1977.
PMID: 890097
We propose the hypothesis that apparently increased risk of leukemia to Fanconi heterozygotes actually represents admixture with the WT syndrome and that Fanconi heterozygotes may not have an increased risk of leukemia....
We propose the hypothesis that apparently increased risk of leukemia to Fanconi heterozygotes actually represents admixture with the WT …
Item in Clipboard
Cite
Cite