Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

139 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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>;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.
139 results
Jump to page