De Braekeleer M - Search Results

1

A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec.

Merante F, Petrova-Benedict R, MacKay N, Mitchell G, Lambert M, Morin C, De Braekeleer M, Laframboise R, Gagné R, Robinson BH. Merante F, et al. Among authors: de braekeleer m. Am J Hum Genet. 1993 Aug;53(2):481-7. Am J Hum Genet. 1993. PMID: 8392290 Free PMC article.

2

Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean.

Morin C, Mitchell G, Larochelle J, Lambert M, Ogier H, Robinson BH, De Braekeleer M. Morin C, et al. Among authors: de braekeleer m. Am J Hum Genet. 1993 Aug;53(2):488-96. Am J Hum Genet. 1993. PMID: 8392291 Free PMC article.

3

Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency.

Morin C, Dubé J, Robinson BH, Lacroix J, Michaud J, De Braekeleer M, Geoffroy G, Lortie A, Blanchette C, Lambert MA, Mitchell GA. Morin C, et al. Among authors: de braekeleer m. Ann Neurol. 1999 Mar;45(3):389-92. Ann Neurol. 1999. PMID: 10072055

4

More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians.

Hechtman P, Kaplan F, Bayleran J, Boulay B, Andermann E, de Braekeleer M, Melançon S, Lambert M, Potier M, Gagné R, et al. Hechtman P, et al. Among authors: de braekeleer m. Am J Hum Genet. 1990 Nov;47(5):815-22. Am J Hum Genet. 1990. PMID: 2220821 Free PMC article.

5

Genetic amniocentesis: a six-years experience in an isolated region of northeastern Quebec (Canada).

Hamel G, Simard L, Gagné R, De Braekeleer M. Hamel G, et al. Among authors: de braekeleer m. Genet Couns. 1993;4(2):103-8. Genet Couns. 1993. PMID: 7689325

6

Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada).

Dionne C, Gagné C, Julien P, Murthy MR, Lambert M, Roederer G, Davignon J, Hayden MR, Lupien PJ, de Braekeleer M. Dionne C, et al. Among authors: de braekeleer m. Ann Genet. 1992;35(2):89-92. Ann Genet. 1992. PMID: 1524414

7

Time and space clusters of the French-Canadian M1V phenylketonuria mutation in France.

Lyonnet S, Melle D, de Braekeleer M, Laframboise R, Rey F, John SW, Berthelon M, Berthelot J, Journel H, Le Marec B, et al. Lyonnet S, et al. Among authors: de braekeleer m. Am J Hum Genet. 1992 Jul;51(1):191-6. Am J Hum Genet. 1992. PMID: 1609797 Free PMC article.

8

A study of inbreeding and kinship in intracranial aneurysms in the Saguenay Lac-Saint-Jean region (Quebec, Canada).

De Braekeleer M, Pérusse L, Cantin L, Bouchard JM, Mathieu J. De Braekeleer M, et al. Ann Hum Genet. 1996 Mar;60(2):99-104. doi: 10.1111/j.1469-1809.1996.tb01181.x. Ann Hum Genet. 1996. PMID: 8839125

9

Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families.

Rozen R, Schwartz RH, Hilman BC, Stanislovitis P, Horn GT, Klinger K, Daigneault J, De Braekeleer M, Kerem B, Tsui L, et al. Rozen R, et al. Among authors: de braekeleer m. Am J Hum Genet. 1990 Oct;47(4):606-10. Am J Hum Genet. 1990. PMID: 2220803 Free PMC article.

10

Autosomal recessive disorders in Saguenay-Lac-Saint-Jean (Quebec, Canada): a study of inbreeding.

De Braekeleer M, Gauthier S. De Braekeleer M, et al. Ann Hum Genet. 1996 Jan;60(1):51-6. doi: 10.1111/j.1469-1809.1996.tb01171.x. Ann Hum Genet. 1996. PMID: 8835098

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

298 results

Search Page

Filters