-
An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
PMID: 4134631 [PubMed - indexed for MEDLINE]
-
Cited by 11 PubMed Central articles
-
ReviewJacobsen syndrome.
Mattina T, Perrotta CS, Grossfeld P.
Orphanet J Rare Dis. 2009 Mar 7; 4:9. Epub 2009 Mar 7.
[Orphanet J Rare Dis. 2009]
-
Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.
Tyson C, Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, et al.
Mol Cytogenet. 2008 Nov 11; 1:23. Epub 2008 Nov 11.
[Mol Cytogenet. 2008]
-
FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.
Raslova H, Komura E, Le Couédic JP, Larbret F, Debili N, Feunteun J, Danos O, Albagli O, Vainchenker W, Favier R.
J Clin Invest. 2004 Jul; 114(1):77-84.
[J Clin Invest. 2004]
- » See all...