Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-β
- 1 March 2003
- journal article
- website
- Published by Elsevier in Genetics in Medicine
- Vol. 5 (2) , 113-119
- https://doi.org/10.1097/01.gim.0000056828.03164.30
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/Velo-cardio-facial chromosomal region in 22q11.2Human Molecular Genetics, 1995
- Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2American Journal of Medical Genetics, 1994
- Complementary DNA cloning of the alternatively expressed endothelial cell glycoprotein Ib beta (GPIb beta) and localization of the GPIb beta gene to chromosome 22.Journal of Clinical Investigation, 1994
- Velo‐cardio‐facial syndrome: A review of 120 patientsAmerican Journal of Medical Genetics, 1993
- Deletions and microdeletions of 22q11.2 in velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1992
- A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell linesJournal of Human Genetics, 1992
- Late‐Onset psychosis in the velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1992
- Human platelet glycoprotein IXFEBS Letters, 1990
- A monoclonal antibody to human platelet glycoprotein IIIa detects a related protein in cultured human endothelial cells.Journal of Clinical Investigation, 1985
- A new concept of the cellular basis of immunityThe Journal of Pediatrics, 1965