Weissenbach J - Search Results

1

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians.

Labuda M, Labuda D, Korab-Laskowska M, Cole DE, Zietkiewicz E, Weissenbach J, Popowska E, Pronicka E, Root AW, Glorieux FH. Labuda M, et al. Among authors: weissenbach j. Am J Hum Genet. 1996 Sep;59(3):633-43. Am J Hum Genet. 1996. PMID: 8751865 Free PMC article.

2

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

Casaubon LK, Melanson M, Lopes-Cendes I, Marineau C, Andermann E, Andermann F, Weissenbach J, Prévost C, Bouchard JP, Mathieu J, Rouleau GA. Casaubon LK, et al. Among authors: weissenbach j. Am J Hum Genet. 1996 Jan;58(1):28-34. Am J Hum Genet. 1996. PMID: 8554065 Free PMC article.

3

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F, et al. Doerflinger N, et al. Among authors: weissenbach j. Am J Hum Genet. 1995 May;56(5):1116-24. Am J Hum Genet. 1995. PMID: 7726167 Free PMC article.

4

Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.

Virtaneva K, Miao J, Träskelin AL, Stone N, Warrington JA, Weissenbach J, Myers RM, Cox DR, Sistonen P, de la Chapelle A, et al. Virtaneva K, et al. Among authors: weissenbach j. Am J Hum Genet. 1996 Jun;58(6):1247-53. Am J Hum Genet. 1996. PMID: 8651302 Free PMC article.

5

Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.

Aminoff M, Tahvanainen E, Gräsbeck R, Weissenbach J, Broch H, de la Chapelle A. Aminoff M, et al. Among authors: weissenbach j. Am J Hum Genet. 1995 Oct;57(4):824-31. Am J Hum Genet. 1995. PMID: 7573042 Free PMC article.

6

Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus.

Nikali K, Suomalainen A, Terwilliger J, Koskinen T, Weissenbach J, Peltonen L. Nikali K, et al. Among authors: weissenbach j. Am J Hum Genet. 1995 May;56(5):1088-95. Am J Hum Genet. 1995. PMID: 7726163 Free PMC article.

7

Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q.

van Herwerden L, Rose CS, Reardon W, Brueton LA, Weissenbach J, Malcolm S, Winter RM. van Herwerden L, et al. Among authors: weissenbach j. Am J Hum Genet. 1994 Apr;54(4):669-74. Am J Hum Genet. 1994. PMID: 8128964 Free PMC article.

8

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.

Moisio AL, Sistonen P, Weissenbach J, de la Chapelle A, Peltomäki P. Moisio AL, et al. Among authors: weissenbach j. Am J Hum Genet. 1996 Dec;59(6):1243-51. Am J Hum Genet. 1996. PMID: 8940269 Free PMC article.

9

A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q.

Morissette J, Côté G, Anctil JL, Plante M, Amyot M, Héon E, Trope GE, Weissenbach J, Raymond V. Morissette J, et al. Among authors: weissenbach j. Am J Hum Genet. 1995 Jun;56(6):1431-42. Am J Hum Genet. 1995. PMID: 7762566 Free PMC article.

10

The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6.

Haataja L, Schleutker J, Laine AP, Renlund M, Savontaus ML, Dib C, Weissenbach J, Peltonen L, Aula P. Haataja L, et al. Among authors: weissenbach j. Am J Hum Genet. 1994 Jun;54(6):1042-9. Am J Hum Genet. 1994. PMID: 8198127 Free PMC article.

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