Séréro S - Search Results

Year	Number of Results
1987	1
1988	2
1989	1
1994	1
2005	2
2007	1
2008	2
2009	1
2011	1
2012	2
2017	1
2022	1
2024	0

1

Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin.

Kleinfinger P, Luscan A, Descourvieres L, Buzas D, Boughalem A, Serero S, Valduga M, Trost D, Costa JM, Vivanti AJ, Lohmann L. Kleinfinger P, et al. Among authors: serero s. Genes (Basel). 2022 Nov 3;13(11):2027. doi: 10.3390/genes13112027. Genes (Basel). 2022. PMID: 36360264 Free PMC article.

2

Prenatal forehead edema in 4p- deletion: the 'Greek warrior helmet' profile revisited.

Levaillant JM, Touboul C, Sinico M, Vergnaud A, Serero S, Druart L, Blondeau JR, Abd Alsamad I, Haddad B, Gérard-Blanluet M. Levaillant JM, et al. Among authors: serero s. Prenat Diagn. 2005 Dec;25(12):1150-5. doi: 10.1002/pd.1246. Prenat Diagn. 2005. PMID: 16258951 Review.

3

Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.

Delahaye A, Khung-Savatovsky S, Aboura A, Guimiot F, Drunat S, Alessandri JL, Gérard M, Bitoun P, Boumendil J, Robin S, Huel C, Guilherme R, Serero S, Gressens P, Elion J, Verloes A, Benzacken B, Delezoide AL, Pipiras E. Delahaye A, et al. Among authors: serero s. Am J Med Genet A. 2012 Oct;158A(10):2430-8. doi: 10.1002/ajmg.a.35548. Epub 2012 Aug 17. Am J Med Genet A. 2012. PMID: 22903608

4

Trisomy 13 by robertsonian translocation rob (13;13)(q10;q10) +13: about one case.

Laudat A, Serero S, Seridi I, Burc-Struxiano L. Laudat A, et al. Among authors: serero s. Ann Biol Clin (Paris). 2017 Dec 1;75(6):695-698. doi: 10.1684/abc.2017.1296. Ann Biol Clin (Paris). 2017. PMID: 29043983 Free article. English.

5

De novo subtelomeric deletion additional to an inherited apparently balanced reciprocal translocation.

Delahaye A, Pipiras E, Kanafani S, Touboul C, Vergnaud A, Encha-Razavi F, Sinico M, Benkhalifa M, Kasakyan S, Serero S, Wolf JP, Gérard-Blanluet M, Benzacken B. Delahaye A, et al. Among authors: serero s. Fetal Diagn Ther. 2007;22(4):306-12. doi: 10.1159/000100797. Epub 2007 Mar 15. Fetal Diagn Ther. 2007. PMID: 17361086

6

Mapping of the gene for anti-müllerian hormone to the short arm of human chromosome 19.

Cohen-Haguenauer O, Picard JY, Mattéi MG, Serero S, Nguyen VC, de Tand MF, Guerrier D, Hors-Cayla MC, Josso N, Frézal J. Cohen-Haguenauer O, et al. Among authors: serero s. Cytogenet Cell Genet. 1987;44(1):2-6. doi: 10.1159/000132332. Cytogenet Cell Genet. 1987. PMID: 3028714

7

Prenatal BACs-on-Beads™ : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.

Vialard F, Simoni G, Aboura A, De Toffol S, Molina Gomes D, Marcato L, Serero S, Clement P, Bouhanna P, Rouleau E, Grimi B, Selva J, Gaetani E, Maggi F, Joseph A, Benzacken B, Grati FR. Vialard F, et al. Among authors: serero s. Prenat Diagn. 2011 May;31(5):500-8. doi: 10.1002/pd.2727. Epub 2011 Mar 14. Prenat Diagn. 2011. PMID: 21404304

8

Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization.

Cacheux V, Tachdjian G, Druart L, Oury JF, Sérero S, Blot P, Nessmann C. Cacheux V, et al. Among authors: serero s. Prenat Diagn. 1994 Feb;14(2):79-86. doi: 10.1002/pd.1970140202. Prenat Diagn. 1994. PMID: 8183853

9

Maternal serum screening in cases of mosaic and translocation Down syndrome.

Dreux S, Olivier C, Dupont JM, Leporrier N; Study Group; Oury JF, Muller F. Dreux S, et al. Prenat Diagn. 2008 Aug;28(8):699-703. doi: 10.1002/pd.2051. Prenat Diagn. 2008. PMID: 18615544

10

Assignment of the human fast skeletal muscle myosin alkali light chains gene (MLC1F/MLC3F) to 2q 32.1-2qter.

Cohen-Haguenauer O, Barton PJ, Nguyen VC, Serero S, Gross MS, Jegou-Foubert C, de Tand MF, Robert B, Buckingham M, Frézal J. Cohen-Haguenauer O, et al. Among authors: serero s. Hum Genet. 1988 Jan;78(1):65-70. doi: 10.1007/BF00291237. Hum Genet. 1988. PMID: 3422212

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