Sinet PM - Search Results

1

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

Delabar JM, Theophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Sinet PM. Delabar JM, et al. Among authors: sinet pm. Eur J Hum Genet. 1993;1(2):114-24. doi: 10.1159/000472398. Eur J Hum Genet. 1993. PMID: 8055322

2

No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

Pangalos C, Théophile D, Sinet PM, Marks A, Stamboulieh-Abazis D, Chettouh Z, Prieur M, Verellen C, Rethoré MO, Lejeune J, et al. Pangalos C, et al. Among authors: sinet pm. Am J Hum Genet. 1992 Dec;51(6):1240-50. Am J Hum Genet. 1992. PMID: 1463008 Free PMC article.

3

New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region.

Yaspo ML, Crété N, Chettouh Z, Blouin JL, Rahmani Z, Stehelin D, Sinet PM, Créau-Goldberg N, Delabar JM. Yaspo ML, et al. Among authors: sinet pm. Hum Genet. 1992 Dec;90(4):427-34. doi: 10.1007/BF00220472. Hum Genet. 1992. PMID: 1483701

4

Gene-dosage mapping of 30 DNA markers on chromosome 21.

Delabar JM, Chettouh Z, Rahmani Z, Theophile D, Blouin JL, Bono R, Kraus J, Barton J, Patterson D, Sinet PM. Delabar JM, et al. Among authors: sinet pm. Genomics. 1992 Jul;13(3):887-9. doi: 10.1016/0888-7543(92)90177-t. Genomics. 1992. PMID: 1639420

5

Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21.

Blouin JL, Aurias A, Créau-Goldberg N, Apiou F, Alcaide-Loridan C, Bruel A, Prieur M, Kraus J, Delabar JM, Sinet PM. Blouin JL, et al. Among authors: sinet pm. Hum Genet. 1991 Dec;88(2):167-74. doi: 10.1007/BF00206066. Hum Genet. 1991. PMID: 1684564

6

Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.

Blouin JL, Rahmani Z, Chettouh Z, Prieur M, Fermanian J, Poissonnier M, Leonard C, Nicole A, Mattei JF, Sinet PM, et al. Blouin JL, et al. Among authors: sinet pm. Am J Hum Genet. 1990 Mar;46(3):518-26. Am J Hum Genet. 1990. PMID: 1968705 Free PMC article.

7

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.

Chettouh Z, Croquette MF, Delobel B, Gilgenkrants S, Leonard C, Maunoury C, Prieur M, Rethoré MO, Sinet PM, Chery M, et al. Chettouh Z, et al. Among authors: sinet pm. Am J Hum Genet. 1995 Jul;57(1):62-71. Am J Hum Genet. 1995. PMID: 7611297 Free PMC article.

8

Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.

Sinet PM, Théophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Delabar JM. Sinet PM, et al. Biomed Pharmacother. 1994;48(5-6):247-52. doi: 10.1016/0753-3322(94)90140-6. Biomed Pharmacother. 1994. PMID: 7999986

9

Mapping the Down syndrome chromosome region. Establishment of a YAC contig spanning 1.2 megabases.

Crété N, Gosset P, Théophile D, Duterque-Coquillaud M, Blouin JL, Vayssettes C, Sinet PM, Créau-Goldberg N. Crété N, et al. Among authors: sinet pm. Eur J Hum Genet. 1993;1(1):51-63. doi: 10.1159/000472387. Eur J Hum Genet. 1993. PMID: 8069651

10

Molecular mapping of the Down syndrome phenotype on chromosome 21.

Sinet PM, Théophile D, Rahmani Z, Chettouh Z, Blouin JL, Prieur M, Noel B, Delabar JM. Sinet PM, et al. Prog Clin Biol Res. 1993;384:63-86. Prog Clin Biol Res. 1993. PMID: 8115408 No abstract available.

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