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Fluorometric assay of neuraminidase with a sodium (4-methylumbelliferyl-alpha-D-N-acetylneuraminate) substrate.
Potier M, Mameli L, Bélisle M, Dallaire L, Melançon SB. Potier M, et al. Among authors: dallaire l. Anal Biochem. 1979 Apr 15;94(2):287-96. doi: 10.1016/0003-2697(79)90362-2. Anal Biochem. 1979. PMID: 464297 No abstract available.
Neuraminidase in cultured fibroblasts and leucocytes of homozygotes and heterozygotes for the mucolipidosis II gene (I-cell disease).
Potier M, Melançon SB, Dallaire L, Chicoine R, Mameli L, Bélisle M. Potier M, et al. Among authors: dallaire l. Am J Med Genet. 1979;4(2):191-200. doi: 10.1002/ajmg.1320040211. Am J Med Genet. 1979. PMID: 517575
New autosomal recessive form of amelia.
Michaud J, Filiatrault D, Dallaire L, Lambert M. Michaud J, et al. Among authors: dallaire l. Am J Med Genet. 1995 Mar 27;56(2):164-7. doi: 10.1002/ajmg.1320560210. Am J Med Genet. 1995. PMID: 7625439 Review.
Neuraminidase activity in the mucolipidoses (types I, II and III) and the cherry-red spot myoclonus syndrome.
Potier M, Beauregard G, Bélisle M, Mameli L, Hong VN, Melançon SB, Dallaire L. Potier M, et al. Among authors: dallaire l. Clin Chim Acta. 1979 Dec 3;99(2):97-105. doi: 10.1016/0009-8981(79)90031-7. Clin Chim Acta. 1979. PMID: 574433
Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe.
Sinnett D, Lavergne L, Melançon SB, Dallaire L, Potier M, Labuda D. Sinnett D, et al. Among authors: dallaire l. Hum Genet. 1988 Dec;81(1):4-8. doi: 10.1007/BF00283719. Hum Genet. 1988. PMID: 2904404
A syndrome of generalized elastic fiber deficiency with leprechaunoid features: a distinct genetic disease with an autosomal recessive mode of inheritance.
Dallaire L, Cantin M, Melançon SB, Perreault G, Potier M. Dallaire L, et al. Clin Genet. 1976 Jul;10(1):1-11. doi: 10.1111/j.1399-0004.1976.tb00001.x. Clin Genet. 1976. PMID: 949858
Fragile site and interstitial telomere repeat sequences at the fusion point of a de novo (Y;13) translocation.
Boutouil M, Fetni R, Qu J, Dallaire L, Richer CL, Lemieux N. Boutouil M, et al. Among authors: dallaire l. Hum Genet. 1996 Sep;98(3):323-7. doi: 10.1007/s004390050216. Hum Genet. 1996. PMID: 8707303
Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
Tihy F, Lemyre E, Dallaire L, Lemieux N. Tihy F, et al. Among authors: dallaire l. Am J Med Genet. 2000 Apr 24;91(5):383-6. doi: 10.1002/(sici)1096-8628(20000424)91:5<383::aid-ajmg12>3.0.co;2-g. Am J Med Genet. 2000. PMID: 10767003
De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.
Tihy F, Lemyre E, Lemieux N, Dallaire L. Tihy F, et al. Among authors: dallaire l. Am J Med Genet. 1999 Dec 3;87(4):302-5. Am J Med Genet. 1999. PMID: 10588834 Review.
Club foot, an adverse outcome of early amniocentesis: disruption or deformation? CEMAT. Canadian Early and Mid-Trimester Amniocentesis Trial.
Farrell SA, Summers AM, Dallaire L, Singer J, Johnson JA, Wilson RD. Farrell SA, et al. Among authors: dallaire l. J Med Genet. 1999 Nov;36(11):843-6. J Med Genet. 1999. PMID: 10544229 Free PMC article. Clinical Trial.
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