Couillin P - Search Results

1

More precise localization of the gene for Hunter syndrome.

Le Guern E, Couillin P, Oberlé I, Ravise N, Boue J. Le Guern E, et al. Among authors: couillin p. Genomics. 1990 Jul;7(3):358-62. doi: 10.1016/0888-7543(90)90169-u. Genomics. 1990. PMID: 2114352

2

Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic map.

Couillin P, Le Guern E, Vignal A, Fizames C, Ravisé N, Delportes D, Reguigne I, Rosier MF, Junien C, van Heyningen V, et al. Couillin P, et al. Genomics. 1994 May 15;21(2):379-87. doi: 10.1006/geno.1994.1280. Genomics. 1994. PMID: 8088833

3

Strategy for constructing somatic hybrids isolating the two derivative chromosomes in X;autosome translocations. Application to a female patient t(X;5) with Hunter syndrome.

Couillin P, Le Guern E, Ravise N, Grisard MC, Oostra BA, Boue A. Couillin P, et al. Ann Genet. 1990;33(4):196-207. Ann Genet. 1990. PMID: 2128908

4

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.

Couillin P, Azoulay M, Henry I, Ravisé N, Grisard MC, Jeanpierre C, Barichard F, Metezeau P, Candelier JJ, Lewis W, et al. Couillin P, et al. Hum Genet. 1989 May;82(2):171-8. doi: 10.1007/BF00284053. Hum Genet. 1989. PMID: 2722195

5

Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients.

Plougastel B, Couillin P, Blanquet V, Le Guern E, Bakker E, Turleau C, De Grouchy J, Créau-Goldberg N. Plougastel B, et al. Among authors: couillin p. Genomics. 1992 Oct;14(2):523-5. doi: 10.1016/s0888-7543(05)80259-9. Genomics. 1992. PMID: 1427872

6

Molecular studies of a translocated (X;22) DiGeorge patient using somatic cell hybridization.

Couillin P, Zucman J, Le Guern E, Reguigne I, Grisard MC, Delattre O, Novelli G, Dallapiccola B, Boué A. Couillin P, et al. Ann Genet. 1992;35(3):140-5. Ann Genet. 1992. PMID: 1466562

7

[HLA and molar pregnancies (triploidies, hydatidiform moles and choriocarcinoma). Etiological and epidemiological study].

Couillin P, Ravisé N, Afoutou JM, Chaïbi R, Azoulay M, Hors J, Oury JF, Boué J, Boué A. Couillin P, et al. Ann Genet. 1987;30(4):197-208. Ann Genet. 1987. PMID: 3501264 French.

8

Early prenatal diagnosis of 21-hydroxylase deficiency using amniotic fluid 17-hydroxyprogesterone determination and DNA probes.

Raux-Demay M, Mornet E, Boue J, Couillin P, Oury JF, Ravise N, Deluchat C, Boue A. Raux-Demay M, et al. Among authors: couillin p. Prenat Diagn. 1989 Jul;9(7):457-66. doi: 10.1002/pd.1970090702. Prenat Diagn. 1989. PMID: 2788885

9

Chromosome 11q localization of one of the three expected genes for the human alpha-3-fucosyltransferases, by somatic hybridization.

Couillin P, Mollicone R, Grisard MC, Gibaud A, Ravisé N, Feingold J, Oriol R. Couillin P, et al. Cytogenet Cell Genet. 1991;56(2):108-11. doi: 10.1159/000133061. Cytogenet Cell Genet. 1991. PMID: 1672847

10

The gene for catalase is assigned between the antigen loci MIC4 and MIC11.

Couillin P, Azoulay M, Metezeau P, Grisard MC, Junien C. Couillin P, et al. Genomics. 1989 Jan;4(1):7-11. doi: 10.1016/0888-7543(89)90307-8. Genomics. 1989. PMID: 2536636

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