Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
- 1 February 1983
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 102 (2), 224-227
- https://doi.org/10.1016/s0022-3476(83)80525-3
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Factor XIIIMedicine, 1979
- Noonan syndrome in an adult family presenting with chronic lymphedemaAmerican Journal Of Medicine, 1978
- High gene frequency of factor XI (PTA) deficiency in Ashkenazi JewsBlood, 1978
- Plasma thromboplastin antecedent (PTA, factor XI): a specific and sensitive radioimmunoassayBlood, 1977
- Factor XI activity and factor XI antigen in homozygous and heterozygous factor XI deficiencyBlood, 1976
- The Noonan Syndrome: A Family StudyAnnals of Internal Medicine, 1974
- Hypertelorism With Turner PhenotypeAmerican Journal of Diseases of Children, 1968
- The Measurement of Factor XI (Plasma Thromboplastin Antecedent)British Journal of Haematology, 1966