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Hereditary Tyrosinemia in a French Canadian Isolate

Overview
Journal Am J Hum Genet
Publisher Cell Press
Specialty Genetics
Date 1969 Jan 1
PMID 5763606
Citations 13
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References
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La Du B . The enzymatic deficiency in tyrosinemia. Am J Dis Child. 1967; 113(1):54-7. DOI: 10.1001/archpedi.1967.02090160104010. View

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Li C . Segregation of the Ellis-van Creveld Syndrome as Analyzed by the First Appearance Method. Am J Hum Genet. 1965; 17(4):343-51. PMC: 1932620. View

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Larochelle J, Mortezai A, Belanger M, Tremblay M, CLAVEAU J, Aubin G . Experience with 37 infants with tyrosinemia. Can Med Assoc J. 1967; 97(18):1051-4. PMC: 1923562. View

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MCKUSICK V, Egeland J, Eldridge R, KRUSEN D . DWARFISM IN THE AMISH I. THE ELLIS-VAN CREVELD SYNDROME. Bull Johns Hopkins Hosp. 1964; 115:306-36. View

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Scriver C, Larochelle J, Silverberg M . Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate. Am J Dis Child. 1967; 113(1):41-6. DOI: 10.1001/archpedi.1967.02090160091008. View