Sinet PM - Search Results

1

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.

Lyle R, Béna F, Gagos S, Gehrig C, Lopez G, Schinzel A, Lespinasse J, Bottani A, Dahoun S, Taine L, Doco-Fenzy M, Cornillet-Lefèbvre P, Pelet A, Lyonnet S, Toutain A, Colleaux L, Horst J, Kennerknecht I, Wakamatsu N, Descartes M, Franklin JC, Florentin-Arar L, Kitsiou S, Aït Yahya-Graison E, Costantine M, Sinet PM, Delabar JM, Antonarakis SE. Lyle R, et al. Among authors: sinet pm. Eur J Hum Genet. 2009 Apr;17(4):454-66. doi: 10.1038/ejhg.2008.214. Epub 2008 Nov 12. Eur J Hum Genet. 2009. PMID: 19002211 Free PMC article.

2

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

3

Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality.

Huret JL, Delabar JM, Marlhens F, Aurias A, Nicole A, Berthier M, Tanzer J, Sinet PM. Huret JL, et al. Among authors: sinet pm. Hum Genet. 1987 Mar;75(3):251-7. doi: 10.1007/BF00281069. Hum Genet. 1987. PMID: 2951317

4

Submicroscopic duplication of chromosome 21 and trisomy 21 phenotype (Down syndrome).

Delabar JM, Sinet PM, Chadefaux B, Nicole A, Gegonne A, Stehelin D, Fridlansky F, Créau-Goldberg N, Turleau C, de Grouchy J. Delabar JM, et al. Among authors: sinet pm. Hum Genet. 1987 Jul;76(3):225-9. doi: 10.1007/BF00283612. Hum Genet. 1987. PMID: 3036686

5

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

6

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

7

High-resolution physical mapping of a 6.7-Mb YAC contig spanning a region critical for the monosomy 21 phenotype in 21q21.3-q22.1.

Orti R, Mégarbane A, Maunoury C, Van Broeckhoven C, Sinet PM, Delabar JM. Orti R, et al. Among authors: sinet pm. Genomics. 1997 Jul 1;43(1):25-33. doi: 10.1006/geno.1997.4765. Genomics. 1997. PMID: 9226369

8

Partial physical map of human chromosome 21 from fibroblast and lymphocyte DNA.

Crété N, Delabar JM, Rahmani Z, Yaspo ML, Kraus J, Marks A, Sinet PM, Créau-Goldberg N. Crété N, et al. Among authors: sinet pm. Hum Genet. 1993 Apr;91(3):245-53. doi: 10.1007/BF00218265. Hum Genet. 1993. PMID: 8478008

9

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.

10

Developmentally regulated expression of mtprd, the murine ortholog of tprd, a gene from the Down syndrome chromosomal region 1.

Lopes C, Rachidi M, Gassanova S, Sinet PM, Delabar JM. Lopes C, et al. Among authors: sinet pm. Mech Dev. 1999 Jun;84(1-2):189-93. doi: 10.1016/s0925-4773(99)00076-3. Mech Dev. 1999. PMID: 10473140 Free article.

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