Noonan syndrome.
Open Access
- 1 January 1987
- journal article
- review article
- Published by BMJ in Journal of Medical Genetics
- Vol. 24 (1) , 9-13
- https://doi.org/10.1136/jmg.24.1.9
Abstract
No abstract availableThis publication has 38 references indexed in Scilit:
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- Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndromeThe Journal of Pediatrics, 1983
- Teratogenic effects associated with maternal primidone therapyThe Journal of Pediatrics, 1981
- Familial Williams SyndromeClinical Genetics, 1980
- Keratosis pilaris atrophicans faciei (Ulerythema ophryogenes): a cutaneous marker in the Noonan syndromeBritish Journal of Dermatology, 1979
- Malignant hyperthermia associated with myopathy and normal muscle enzymesThe Journal of Pediatrics, 1977
- Congenital stem cell dysfunction associated with Turner-like phenotypeThe Journal of Pediatrics, 1976
- An evaluation of the possible association of malignant hyperpyrexia with the Noonan syndrome using serum creatine phosphokinase levelsThe Journal of Pediatrics, 1975
- Noonan's syndrome and autoimmune thyroiditisThe Journal of Pediatrics, 1973
- Anesthetic-induced malignant hyperpyrexia in childrenThe Journal of Pediatrics, 1973