Hanauer A - Search Results

1

Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2; q11.2) primary change in synovial sarcomas.

Gilgenkrantz S, Chery M, Teboul M, Mujica P, Leotard B, Gregoire MJ, Boman F, Duprez A, Hanauer A. Gilgenkrantz S, et al. Among authors: hanauer a. Oncogene. 1990 Jul;5(7):1063-6. Oncogene. 1990. PMID: 2165233

2

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

3

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.

4

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

5

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

6

Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.

Walder RY, Shalev H, Brennan TM, Carmi R, Elbedour K, Scott DA, Hanauer A, Mark AL, Patil S, Stone EM, Sheffield VC. Walder RY, et al. Among authors: hanauer a. Hum Mol Genet. 1997 Sep;6(9):1491-7. doi: 10.1093/hmg/6.9.1491. Hum Mol Genet. 1997. PMID: 9285786

7

Genetic analysis of new French X-linked juvenile retinoschisis kindreds using microsatellite markers closely linked to the RS locus: further narrowing of the RS candidate region.

Dumur V, Trivier E, Puech B, Peugnet F, Zanlonghi X, Hache JC, Hanauer A. Dumur V, et al. Among authors: hanauer a. Hum Genet. 1995 Jul;96(1):79-82. doi: 10.1007/BF00214190. Hum Genet. 1995. PMID: 7607659

8

Activation of RSK by UV-light: phosphorylation dynamics and involvement of the MAPK pathway.

Mérienne K, Jacquot S, Zeniou M, Pannetier S, Sassone-Corsi P, Hanauer A. Mérienne K, et al. Among authors: hanauer a. Oncogene. 2000 Aug 31;19(37):4221-9. doi: 10.1038/sj.onc.1203712. Oncogene. 2000. PMID: 10980595

9

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

10

Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations.

de la Salle C, Wu Q, Baas MJ, Hanauer A, Ruan C, Cazenave JP. de la Salle C, et al. Among authors: hanauer a. Clin Genet. 1990 Dec;38(6):434-40. doi: 10.1111/j.1399-0004.1990.tb03609.x. Clin Genet. 1990. PMID: 1981181

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