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- Beck M., Glössl J., Rüter R., Kresse H. Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome. Pediatr Res. 1983 Nov;17(11):926–929. doi: 10.1203/00006450-198311000-00018. [DOI] [PubMed] [Google Scholar]
- Collacott R. A., Warrington J. S., Young I. D. Coffin-Lowry syndrome and schizophrenia: a family report. J Ment Defic Res. 1987 Jun;31(Pt 2):199–207. doi: 10.1111/j.1365-2788.1987.tb01356.x. [DOI] [PubMed] [Google Scholar]
- Fryns J. P., Vinken L., Van den Berghe H. The Coffin syndrome. Hum Genet. 1977 May 10;36(3):271–276. doi: 10.1007/BF00446276. [DOI] [PubMed] [Google Scholar]
- Haspeslagh M., Fryns J. P., Beusen L., Van Dessel F., Vinken L., Moens E., Van den Berghe H. The Coffin-Lowry syndrome. A study of two new index patients and their families. Eur J Pediatr. 1984 Dec;143(2):82–86. doi: 10.1007/BF00445790. [DOI] [PubMed] [Google Scholar]
- Hersh J. H., Weisskopf B., DeCoster C. Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clue. Am J Med Genet. 1984 Jun;18(2):195–199. doi: 10.1002/ajmg.1320180203. [DOI] [PubMed] [Google Scholar]
- Hunter A. G., Partington M. W., Evans J. A. The Coffin-Lowry syndrome. Experience from four centres. Clin Genet. 1982 May;21(5):321–335. doi: 10.1111/j.1399-0004.1982.tb01379.x. [DOI] [PubMed] [Google Scholar]
- Kousseff B. G. Coffin-Lowry syndrome in an Afro-American family. Am J Med Genet. 1982 Mar;11(3):373–375. doi: 10.1002/ajmg.1320110317. [DOI] [PubMed] [Google Scholar]
- Lowry B., Miller J. R., Fraser F. C. A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus. Am J Dis Child. 1971 Jun;121(6):496–500. [PubMed] [Google Scholar]
- Martinelli B., Campailla E. Contributo alla conoscenza della sindrome di Coffin, Siris, Wegienka. G Psichiatr Neuropatol. 1969;97(3):449–458. [PubMed] [Google Scholar]
- Merchant R. H. The Coffin-Lowry syndrome: a facio digital mental retardation syndrome: a case report. Indian Pediatr. 1976 Mar;13(3):247–249. [PubMed] [Google Scholar]
- Procopis P. G., Turner B. Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's syndrome. Am J Dis Child. 1972 Aug;124(2):258–261. doi: 10.1001/archpedi.1972.02110140108016. [DOI] [PubMed] [Google Scholar]
- Salinas C. F. Orodental findings and genetic disorders. Birth Defects Orig Artic Ser. 1982;18(1):79–120. [PubMed] [Google Scholar]
- Sylvester P. E., Rundle A. T., Richards B. W. The syndrome of Coffin, Siris and Wegienka: report of a case. J Ment Defic Res. 1976 Mar;20(1):35–54. doi: 10.1111/j.1365-2788.1976.tb00015.x. [DOI] [PubMed] [Google Scholar]
- Temtamy S. A., Miller J. D., Hussels-Maumenee I. The Coffin-Lowry syndrome: an inherited faciodigital mental retardation syndrome. J Pediatr. 1975 May;86(5):724–731. doi: 10.1016/s0022-3476(75)80357-x. [DOI] [PubMed] [Google Scholar]
- Wilson W. G., Kelly T. E. Brief clinical report: early recognition of the Coffin-Lowry syndrome. Am J Med Genet. 1981;8(2):215–220. doi: 10.1002/ajmg.1320080212. [DOI] [PubMed] [Google Scholar]