Beckmann J - Search Results

1

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

Medhioub M, Cherif D, Benessy F, Silbermann F, Gubler MC, Le Paslier D, Cohen D, Weissenbach J, Beckmann J, Antignac C. Medhioub M, et al. Among authors: beckmann j. Genomics. 1994 Jul 15;22(2):296-301. doi: 10.1006/geno.1994.1387. Genomics. 1994. PMID: 7806215

2

A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p.

Antignac C, Arduy CH, Beckmann JS, Benessy F, Gros F, Medhioub M, Hildebrandt F, Dufier JL, Kleinknecht C, Broyer M, et al. Antignac C, et al. Among authors: beckmann js. Nat Genet. 1993 Apr;3(4):342-5. doi: 10.1038/ng0493-342. Nat Genet. 1993. PMID: 7981755

3

Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

Fuchshuber A, Jean G, Gribouval O, Gubler MC, Broyer M, Beckmann JS, Niaudet P, Antignac C. Fuchshuber A, et al. Among authors: beckmann js. Hum Mol Genet. 1995 Nov;4(11):2155-8. doi: 10.1093/hmg/4.11.2155. Hum Mol Genet. 1995. PMID: 8589695

4

Mapping of two chromosome 15 microsatellites.

Fougerousse F, Richard I, Broux O, Cohen D, Beckmann JS. Fougerousse F, et al. Among authors: beckmann js. Genomics. 1992 Jul;13(3):903-4. doi: 10.1016/0888-7543(92)90184-t. Genomics. 1992. PMID: 1639425 No abstract available.

5

Targeted development of microsatellite markers from inter-Alu amplification of YAC clones.

de Souza AP, Allamand V, Richard I, Brenguier L, Chumakov I, Cohen D, Beckmann JS. de Souza AP, et al. Among authors: beckmann js. Genomics. 1994 Jan 15;19(2):391-3. doi: 10.1006/geno.1994.1079. Genomics. 1994. PMID: 8188274

6

The gene for creatine kinase, mitochondrial 2 (sarcomeric; CKMT2), maps to chromosome 5q13.3.

Richard I, Devaud C, Cherif D, Cohen D, Beckmann JS. Richard I, et al. Among authors: beckmann js. Genomics. 1993 Oct;18(1):134-6. doi: 10.1006/geno.1993.1437. Genomics. 1993. PMID: 8276398

7

Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy.

Richard I, Broux O, Hillaire D, Cherif D, Fougerousse F, Cohen D, Beckmann JS. Richard I, et al. Among authors: beckmann js. Hum Mol Genet. 1992 Nov;1(8):621-4. doi: 10.1093/hmg/1.8.621. Hum Mol Genet. 1992. PMID: 1363783

8

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites.

Beckmann JS, Tomfohrde J, Barnes RI, Williams M, Broux O, Richard I, Weissenbach J, Bowcock AM. Beckmann JS, et al. Hum Mol Genet. 1993 Dec;2(12):2019-30. doi: 10.1093/hmg/2.12.2019. Hum Mol Genet. 1993. PMID: 7906587

9

A first high-density map of 981 biallelic markers on human chromosome 14.

Escary JL, Bottius E, Prince N, Reyes C, Fiawoumo Y, Caloustian C, Bruls T, Fujiyama A, Cooper RS, Adeyemo AA, Lathrop GM, Weissenbach J, Gyapay G, Foglio M, Beckmann JS. Escary JL, et al. Among authors: beckmann js. Genomics. 2000 Dec 1;70(2):153-64. doi: 10.1006/geno.2000.6369. Genomics. 2000. PMID: 11112343

10

Exclusion of genes coding for proteins of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach.

Dufour C, Carrier L, Hengstenberg C, Bercovici J, Dausse E, Weissenbach J, Dubourg O, Komajda M, Schwartz K, Beckmann JS. Dufour C, et al. Among authors: beckmann js. C R Acad Sci III. 1993;316(5):474-81. C R Acad Sci III. 1993. PMID: 8221230

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