Hanauer A - Search Results

1

Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.

Biancalana V, Le Marec B, Odent S, van den Hurk JA, Hanauer A. Biancalana V, et al. Among authors: hanauer a. Hum Genet. 1991 Dec;88(2):228-30. doi: 10.1007/BF00206078. Hum Genet. 1991. PMID: 1757098

2

X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.

Piussan C, Hanauer A, Dahl N, Mathieu M, Kolski C, Biancalana V, Heyberger S, Strunski V. Piussan C, et al. Among authors: hanauer a. Am J Hum Genet. 1995 Jan;56(1):224-30. Am J Hum Genet. 1995. PMID: 7825582 Free PMC article.

3

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.

Biancalana V, Serville F, Pommier J, Julien J, Hanauer A, Mandel JL. Biancalana V, et al. Among authors: hanauer a. Hum Mol Genet. 1992 Jul;1(4):255-8. doi: 10.1093/hmg/1.4.255. Hum Mol Genet. 1992. PMID: 1303195

4

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

5

Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.

Chery M, Biancalana V, Philippe C, Malpuech G, Carla H, Gilgenkrantz S, Mandel JL, Hanauer A. Chery M, et al. Among authors: hanauer a. Hum Genet. 1994 May;93(5):587-91. doi: 10.1007/BF00202829. Hum Genet. 1994. PMID: 8168840

6

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

7

Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.

Hanauer A, Alembik Y, Arveiler B, Formiga L, Gilgenkrantz S, Mandel JL. Hanauer A, et al. Hum Genet. 1988 Oct;80(2):177-80. doi: 10.1007/BF00702863. Hum Genet. 1988. PMID: 2902000

8

Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations.

Jacquot S, Merienne K, De Cesare D, Pannetier S, Mandel JL, Sassone-Corsi P, Hanauer A. Jacquot S, et al. Among authors: hanauer a. Am J Hum Genet. 1998 Dec;63(6):1631-40. doi: 10.1086/302153. Am J Hum Genet. 1998. PMID: 9837815 Free PMC article.

9

The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.

Hanauer A, Chery M, Fujita R, Driesel AJ, Gilgenkrantz S, Mandel JL. Hanauer A, et al. Am J Hum Genet. 1990 Jan;46(1):133-7. Am J Hum Genet. 1990. PMID: 2294745 Free PMC article.

10

Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis.

Hanauer A, Alembik Y, Gilgenkrantz S, Mujica P, Nivelon-Chevallier A, Pembrey ME, Young ID, Mandel JL. Hanauer A, et al. Am J Med Genet. 1988 May-Jun;30(1-2):523-30. doi: 10.1002/ajmg.1320300154. Am J Med Genet. 1988. PMID: 3177469

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