Romana SP - Search Results

1

A fertilin-derived peptide improves in vitro maturation and ploidy of human oocytes.

Sallem A, Denizot AL, Ziyyat A, L'Hostis A, Favier S, Burlet P, Lapierre JM, Dimby SF, Patrat C, Sifer C, Vicaut E, Steffann J, Vaiman D, Romana SP, Wolf JP. Sallem A, et al. Among authors: romana sp. F S Sci. 2022 Feb;3(1):21-28. doi: 10.1016/j.xfss.2021.10.004. Epub 2021 Nov 3. F S Sci. 2022. PMID: 35559993 Free article. Clinical Trial.

2

Molecular karyotyping in human constitutional cytogenetics.

Sanlaville D, Lapierre JM, Turleau C, Coquin A, Borck G, Colleaux L, Vekemans M, Romana SP. Sanlaville D, et al. Among authors: romana sp. Eur J Med Genet. 2005 Jul-Sep;48(3):214-31. doi: 10.1016/j.ejmg.2005.04.013. Eur J Med Genet. 2005. PMID: 16179218 Review.

3

Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy.

Leroy C, Jacquemont ML, Doray B, Lamblin D, Cormier-Daire V, Philippe A, Nusbaum S, Patrat C, Steffann J, Colleaux L, Vekemans M, Romana S, Turleau C, Malan V. Leroy C, et al. Clin Genet. 2016 Jan;89(1):68-73. doi: 10.1111/cge.12567. Epub 2015 Mar 5. Clin Genet. 2016. PMID: 25677961

4

PMX2B, a new candidate gene for Hirschsprung's disease.

Benailly HK, Lapierre JM, Laudier B, Amiel J, Attié T, De Blois MC, Vekemans M, Romana SP. Benailly HK, et al. Among authors: romana sp. Clin Genet. 2003 Sep;64(3):204-9. doi: 10.1034/j.1399-0004.2003.00105.x. Clin Genet. 2003. PMID: 12919134

5

De novo inverted duplication 9p21pter involving telomeric repeated sequences.

Sanlaville D, Baumann C, Lapierre JM, Romana S, Collot N, Cacheux V, Turleau C, Tachdjian G. Sanlaville D, et al. Am J Med Genet. 1999 Mar 12;83(2):125-31. doi: 10.1002/(sici)1096-8628(19990312)83:2<125::aid-ajmg8>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10190483 Review.

6

[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: romana sp. 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.

7

A CGH study of 27 patients with CHARGE association.

Sanlaville D, Romana SP, Lapierre JM, Amiel J, Genevieve D, Ozilou C, Le Lorch M, Brisset S, Gosset P, Baumann C, Turleau C, Lyonnet S, Vekemans M. Sanlaville D, et al. Among authors: romana sp. Clin Genet. 2002 Feb;61(2):135-8. doi: 10.1034/j.1399-0004.2002.610208.x. Clin Genet. 2002. PMID: 11940088

8

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. Ann Genet. 1998;41(3):133-40. Ann Genet. 1998. PMID: 9833066

9

[Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].

Romana SP, Gosset P, Elghezal H, Le Lorc'h M, Ozilou C, Lapierre JM, Sanlaville D, Brisset S, Turleau C, Vekemans M. Romana SP, et al. J Gynecol Obstet Biol Reprod (Paris). 2001 Feb;30(1 Suppl):75-9. J Gynecol Obstet Biol Reprod (Paris). 2001. PMID: 11240520 Free article. Review. French. No abstract available.

10

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. Clin Genet. 2001 Sep;60(3):212-9. doi: 10.1034/j.1399-0004.2001.600307.x. Clin Genet. 2001. PMID: 11595023

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