Aurias A - Search Results

1

Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype.

Joly G, Lapierre JM, Ozilou C, Gosset P, Aurias A, de Blois MC, Prieur M, Raoul O, Colleaux L, Munnich A, Romana S, Vekemans M, Turleau C. Joly G, et al. Among authors: aurias a. Clin Genet. 2001 Sep;60(3):212-9. doi: 10.1034/j.1399-0004.2001.600307.x. Clin Genet. 2001. PMID: 11595023

2

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.

Jeanpierre M, Turleau C, Aurias A, Prieur M, Ledeist F, Fischer A, Viegas-Pequignot E. Jeanpierre M, et al. Among authors: aurias a. Hum Mol Genet. 1993 Jun;2(6):731-5. doi: 10.1093/hmg/2.6.731. Hum Mol Genet. 1993. PMID: 8102570

3

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G. Lapierre JM, et al. Among authors: aurias a. Ann Genet. 1998;41(3):133-40. Ann Genet. 1998. PMID: 9833066

4

[Microarray CGH: principle and use for constitutional disorders].

Sanlaville D, Lapierre JM, Coquin A, Turleau C, Vermeesch J, Colleaux L, Borck G, Vekemans M, Aurias A, Romana SP. Sanlaville D, et al. Among authors: aurias a. Arch Pediatr. 2005 Oct;12(10):1515-20. doi: 10.1016/j.arcped.2005.07.014. Epub 2005 Sep 8. Arch Pediatr. 2005. PMID: 16153813 French.

5

Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.

Lapierre JM, Cacheux V, Luton D, Collot N, Oury JF, Aurias A, Tachdjian G. Lapierre JM, et al. Among authors: aurias a. Prenat Diagn. 2000 Feb;20(2):123-31. doi: 10.1002/(sici)1097-0223(200002)20:2<123::aid-pd762>3.0.co;2-b. Prenat Diagn. 2000. PMID: 10694684

6

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: aurias a. Hum Genet. 1991 Dec;88(2):167-74. doi: 10.1007/BF00206066. Hum Genet. 1991. PMID: 1684564

7

The chemotherapeutic drug melphalan induces breakage of chromosomes regions rearranged in secondary leukemia.

Mamuris Z, Prieur M, Dutrillaux B, Aurias A. Mamuris Z, et al. Among authors: aurias a. Cancer Genet Cytogenet. 1989 Jan;37(1):65-77. doi: 10.1016/0165-4608(89)90076-9. Cancer Genet Cytogenet. 1989. PMID: 2917334

8

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization.

Desmaze C, Scambler P, Prieur M, Halford S, Sidi D, Le Deist F, Aurias A. Desmaze C, et al. Among authors: aurias a. Hum Genet. 1993 Feb;90(6):663-5. doi: 10.1007/BF00202489. Hum Genet. 1993. PMID: 8444474

9

Systematic analysis of 95 reciprocal translocations of autosomes.

Aurias A, Prieur M, Dutrillaux B, Lejeune J. Aurias A, et al. Hum Genet. 1978 Dec 29;45(3):259-82. doi: 10.1007/BF00278725. Hum Genet. 1978. PMID: 738728

10

Down syndrome critical region around D21S55 on proximal 21q22.3.

Rahmani Z, Blouin JL, Créau-Goldberg N, Watkins PC, Mattei JF, Poissonnier M, Prieur M, Chettouh Z, Nicole A, Aurias A, et al. Rahmani Z, et al. Among authors: aurias a. Am J Med Genet Suppl. 1990;7:98-103. doi: 10.1002/ajmg.1320370720. Am J Med Genet Suppl. 1990. PMID: 2149984

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