Abbadi N - Search Results

1

Physical mapping of DNA markers in the q13-q22 region of the human X chromosome.

Philippe C, Cremers FP, Chery M, Bach I, Abbadi N, Ropers HH, Gilgenkrantz S. Philippe C, et al. Among authors: abbadi n. Genomics. 1993 Jul;17(1):147-52. doi: 10.1006/geno.1993.1296. Genomics. 1993. PMID: 8406446

2

New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval.

Oberlé I, Vincent A, Abbadi N, Rousseau F, Hupkes PE, Hors-Cayla MC, Gilgenkrantz S, Oostra BA, Mandel JL. Oberlé I, et al. Among authors: abbadi n. Am J Med Genet. 1991 Feb-Mar;38(2-3):336-42. doi: 10.1002/ajmg.1320380234. Am J Med Genet. 1991. PMID: 1673307

3

[Y chromosome rearrangement and phenotypical consequences].

Mujica P, Abbadi N, Formiga LD, Gilgenkrantz S. Mujica P, et al. Among authors: abbadi n. J Genet Hum. 1988 Jan;36(1-2):69-73. J Genet Hum. 1988. PMID: 3379381 French. No abstract available.

4

X chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe.

Camus P, Abbadi N, Perrier MC, Chéry M, Gilgenkrantz S. Camus P, et al. Among authors: abbadi n. Hum Genet. 1996 Feb;97(2):247-50. doi: 10.1007/BF02265275. Hum Genet. 1996. PMID: 8566963

5

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.

Abbadi N, Philippe C, Chery M, Gilgenkrantz H, Tome F, Collin H, Theau D, Recan D, Broux O, Fardeau M, et al. Abbadi N, et al. Am J Med Genet. 1994 Aug 15;52(2):198-206. doi: 10.1002/ajmg.1320520215. Am J Med Genet. 1994. PMID: 7802009

6

X inactivation in Rett syndrome: a preliminary study showing partial preferential inactivation of paternal X with the M27 beta probe.

Camus P, Abbadi N, Gilgenkrantz S. Camus P, et al. Among authors: abbadi n. Am J Med Genet. 1994 Apr 15;50(3):307-8. doi: 10.1002/ajmg.1320500321. Am J Med Genet. 1994. PMID: 8042680 No abstract available.

7

Myoblast transplantation between monozygotic twin girl carriers of Duchenne muscular dystrophy.

Tremblay JP, Bouchard JP, Malouin F, Théau D, Cottrell F, Collin H, Rouche A, Gilgenkrantz S, Abbadi N, Tremblay M, et al. Tremblay JP, et al. Among authors: abbadi n. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):583-92. doi: 10.1016/0960-8966(93)90121-y. Neuromuscul Disord. 1993. PMID: 8186717

8

Mouse chromosome 14.

Abbadi N, Nadeau JH. Abbadi N, et al. Mamm Genome. 1997;7 Spec No:S238-50. doi: 10.1007/s003359900326. Mamm Genome. 1997. PMID: 9233397 No abstract available.

9

Encyclopedia of the mouse genome VII. Mouse chromosome 14.

Abbadi N, Nadeau JH. Abbadi N, et al. Mamm Genome. 1998;8 Spec No:S275-91. doi: 10.1007/s003359900659. Mamm Genome. 1998. PMID: 9662631 No abstract available.

10

Disorganization in mice and humans and its relation to sporadic birth defects.

Robin NH, Abbadi N, McCandless SE, Nadeau JH. Robin NH, et al. Among authors: abbadi n. Am J Med Genet. 1997 Dec 31;73(4):425-36. doi: 10.1002/(sici)1096-8628(19971231)73:4<425::aid-ajmg11>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9415470 Review.

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