Potier M - Search Results

1

[Sandhoff's disease: clinical and genetic study of a French-Canadian child].

Melançon SB, Potier M, Geoffroy G, Dallaire L. Melançon SB, et al. Among authors: potier m. Union Med Can. 1974 Jul;103(7):1218-22. Union Med Can. 1974. PMID: 4210450 French. No abstract available.

2

[Prenatal diagnosis: data on the cell viability and alpha fetoproteins of the amniotic fluid].

Dallaire L, Morin-Gonthier M, Potier M, Melançon SB. Dallaire L, et al. Among authors: potier m. Union Med Can. 1975 Dec;104(12):1782-6. Union Med Can. 1975. PMID: 56074 French. No abstract available.

3

[Biochemical approach to prenatal diagnosis of inborn errors of metabolism and congenital malformations].

Melançon SB, Potier M, Dallaire L. Melançon SB, et al. Among authors: potier m. Union Med Can. 1975 Dec;104(12):1787-90. Union Med Can. 1975. PMID: 1216372 French. No abstract available.

4

[Comparative study of urine and serum organic acids in newborn infants using gas chromatography].

Melançon SB, Grignon B, Dallaire L, Potier M. Melançon SB, et al. Among authors: potier m. Union Med Can. 1974 Apr;103(4):678-85. Union Med Can. 1974. PMID: 4839690 French. No abstract available.

5

[Prenatal diagnosis of genetic diseases. I: indications].

Dallaire L, Melançon SB, Potier M, Gagnon M, Boisvert J, Lortie G. Dallaire L, et al. Among authors: potier m. Union Med Can. 1982 Mar;111(3):189-202. Union Med Can. 1982. PMID: 6177081 French. No abstract available.

6

[Prenatal diagnosis of genetic diseases during the second trimester of pregnancy, II: results].

Dallaire L, Melançon SB, Potier M, Gagnon M, Boisvert J, Lortie G. Dallaire L, et al. Among authors: potier m. Union Med Can. 1982 Apr;111(4):299-310. Union Med Can. 1982. PMID: 6178197 French. No abstract available.

7

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. Among authors: potier m. Clin Genet. 1976 Jul;10(1):1-11. doi: 10.1111/j.1399-0004.1976.tb00001.x. Clin Genet. 1976. PMID: 949858

8

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: potier m. Hum Genet. 1988 Dec;81(1):4-8. doi: 10.1007/BF00283719. Hum Genet. 1988. PMID: 2904404

9

N-Acetyl-beta-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses.

Potier M, Boire G, Dallaire L, Melancon SB. Potier M, et al. Clin Chim Acta. 1977 May 2;76(3):309-15. doi: 10.1016/0009-8981(77)90156-5. Clin Chim Acta. 1977. PMID: 404100

10

Purification and some properties of liver and brain beta-N-acetyl-hexosaminidase S.

Potier M, Teitelbaum J, Melancon SB, Dallaire L. Potier M, et al. Biochim Biophys Acta. 1979 Jan 12;566(1):80-7. doi: 10.1016/0005-2744(79)90251-1. Biochim Biophys Acta. 1979. PMID: 758959

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

495 results

Search Page

Filters