Hanauer A - Search Results

1

Dinucleotide repeat polymorphism at Xq26.1 (DXS1114).

Weber C, Oudet C, Johnson S, Pilia G, Schlessinger D, Hanauer A. Weber C, et al. Among authors: hanauer a. Hum Mol Genet. 1993 May;2(5):612. doi: 10.1093/hmg/2.5.612. Hum Mol Genet. 1993. PMID: 8518807 No abstract available.

2

Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination.

Oudet C, Heilig R, Hanauer A, Mandel JL. Oudet C, et al. Among authors: hanauer a. Am J Hum Genet. 1991 Aug;49(2):311-9. Am J Hum Genet. 1991. PMID: 1867193 Free PMC article.

3

Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene.

Oudet C, Weber C, Kaplan J, Segues B, Croquette MF, Roman EO, Hanauer A. Oudet C, et al. Among authors: hanauer a. J Med Genet. 1993 Apr;30(4):300-3. doi: 10.1136/jmg.30.4.300. J Med Genet. 1993. PMID: 8487275 Free PMC article.

4

Dinucleotide repeat polymorphism close to IDS gene in Xq27.3-q28 (DXS1113).

Weber C, Oudet C, Johnson S, Pilia G, Schlessinger D, Hanauer A. Weber C, et al. Among authors: hanauer a. Hum Mol Genet. 1993 May;2(5):612. doi: 10.1093/hmg/2.5.612-a. Hum Mol Genet. 1993. PMID: 8518808 No abstract available.

5

Two hot spots of recombination in the DMD gene correlate with the deletion prone regions.

Oudet C, Hanauer A, Clemens P, Caskey T, Mandel JL. Oudet C, et al. Among authors: hanauer a. Hum Mol Genet. 1992 Nov;1(8):599-603. doi: 10.1093/hmg/1.8.599. Hum Mol Genet. 1992. PMID: 1363782

6

Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.

Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PS, O'Riordan JL, Partington MW, Heyberger S, Oudet C, Hanauer A. Biancalana V, et al. Among authors: hanauer a. Genomics. 1994 Aug;22(3):617-25. doi: 10.1006/geno.1994.1435. Genomics. 1994. PMID: 8001973

7

A second family with XLRH displays the mutation S244L in the CLCN5 gene.

Oudet C, Martin-Coignard D, Pannetier S, Praud E, Champion G, Hanauer A. Oudet C, et al. Among authors: hanauer a. Hum Genet. 1997 Jun;99(6):781-4. doi: 10.1007/s004390050448. Hum Genet. 1997. PMID: 9187673

8

New markers for linkage analysis of X-linked hypophosphataemic rickets.

Rowe PS, Goulding J, Read A, Mountford R, Hanauer A, Oudet C, Whyte MP, Meier-Ewert S, Lehrach H, Davies KE, et al. Rowe PS, et al. Among authors: hanauer a. Hum Genet. 1993 Jul;91(6):571-5. doi: 10.1007/BF00205082. Hum Genet. 1993. PMID: 8101831

9

Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2).

Rowe PS, Goulding J, Read A, Lehrach H, Francis F, Hanauer A, Oudet C, Biancalana V, Kooh SW, Davies KE, et al. Rowe PS, et al. Among authors: hanauer a. Hum Genet. 1994 Mar;93(3):291-4. doi: 10.1007/BF00212025. Hum Genet. 1994. PMID: 8125480

10

Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues.

Filisetti D, Ostermann G, von Bredow M, Strom T, Filler G, Ehrich J, Pannetier S, Garnier JM, Rowe P, Francis F, Julienne A, Hanauer A, Econs MJ, Oudet C. Filisetti D, et al. Among authors: hanauer a. Eur J Hum Genet. 1999 Jul;7(5):615-9. doi: 10.1038/sj.ejhg.5200341. Eur J Hum Genet. 1999. PMID: 10439971

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