Delabar JM - Search Results

1

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. Genomics. 1992 Jul;13(3):887-9. doi: 10.1016/0888-7543(92)90177-t. Genomics. 1992. PMID: 1639420

2

3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21.

Dufresne-Zacharia MC, Dahmane N, Theophile D, Orti R, Chettouh Z, Sinet PM, Delabar JM. Dufresne-Zacharia MC, et al. Among authors: delabar jm. Genomics. 1994 Feb;19(3):462-9. doi: 10.1006/geno.1994.1095. Genomics. 1994. PMID: 8188288

3

Report of the Fourth International Workshop on Human Chromosome 21.

Delabar JM, Créau N, Sinet PM, Ritter O, Antonarakis SE, Burmeister M, Chakravarti A, Nizetic D, Ohki M, Patterson D, et al. Delabar JM, et al. Genomics. 1993 Dec;18(3):735-45. doi: 10.1016/s0888-7543(05)80390-8. Genomics. 1993. PMID: 8307590 No abstract available.

4

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: delabar jm. Hum Genet. 1993 Apr;91(3):245-53. doi: 10.1007/BF00218265. Hum Genet. 1993. PMID: 8478008

5

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: delabar jm. Genomics. 1997 Jul 1;43(1):25-33. doi: 10.1006/geno.1997.4765. Genomics. 1997. PMID: 9226369

6

Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome.

Dahmane N, Ghezala GA, Gosset P, Chamoun Z, Dufresne-Zacharia MC, Lopes C, Rabatel N, Gassanova-Maugenre S, Chettouh Z, Abramowski V, Fayet E, Yaspo ML, Korn B, Blouin JL, Lehrach H, Poutska A, Antonarakis SE, Sinet PM, Créau N, Delabar JM. Dahmane N, et al. Among authors: delabar jm. Genomics. 1998 Feb 15;48(1):12-23. doi: 10.1006/geno.1997.5146. Genomics. 1998. PMID: 9503011

7

Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5.

Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM. Orti R, et al. Among authors: delabar jm. Genomics. 2000 Mar 1;64(2):203-10. doi: 10.1006/geno.1999.6109. Genomics. 2000. PMID: 10729227

8

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: delabar jm. Hum Genet. 1992 Dec;90(4):427-34. doi: 10.1007/BF00220472. Hum Genet. 1992. PMID: 1483701

9

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. Among authors: delabar jm. Biomed Pharmacother. 1994;48(5-6):247-52. doi: 10.1016/0753-3322(94)90140-6. Biomed Pharmacother. 1994. PMID: 7999986

10

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. Eur J Hum Genet. 1993;1(2):114-24. doi: 10.1159/000472398. Eur J Hum Genet. 1993. PMID: 8055322

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