Serero S - Search Results

1

Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker.

Valentin M, Ottenwalter A, Serero S, Muller F, Luton D, Ducarme G. Valentin M, et al. Among authors: serero s. Prenat Diagn. 2009 Dec;29(12):1177-9. doi: 10.1002/pd.2381. Prenat Diagn. 2009. PMID: 19816880 No abstract available.

2

Isolated fetal hyperechogenic bowel associated with intra-uterine parvovirus B19 infection.

Jouannic JM, Gavard L, Créquat J, Muller F, Serero S, Bénifla JL, Costa JM. Jouannic JM, et al. Among authors: serero s. Fetal Diagn Ther. 2005 Nov-Dec;20(6):498-500. doi: 10.1159/000086828. Fetal Diagn Ther. 2005. PMID: 16260882

3

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

4

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.

5

Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.

Bélien V, Gérard-Blanluet M, Serero S, Le Dû N, Baumann C, Jacquemont ML, Dupont C, Krabchi K, Drunat S, Elbez A, Janaud JC, Benzacken B, Verloes A, Tabet AC, Aboura A. Bélien V, et al. Among authors: serero s. Am J Med Genet A. 2008 Jul 15;146A(14):1871-4. doi: 10.1002/ajmg.a.32392. Am J Med Genet A. 2008. PMID: 18553551

6

Regional mapping of the human renin gene to 1q32 by in situ hybridization.

Cohen-Haguenauer O, Soubrier F, Van Cong N, Serero S, Turleau C, Jegou C, Gross MS, Corvol P, Frézal J. Cohen-Haguenauer O, et al. Among authors: serero s. Ann Genet. 1989;32(1):16-20. Ann Genet. 1989. PMID: 2665629

7

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

8

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

9

Localization of the active gene of aldolase on chromosome 16, and two aldolase A pseudogenes on chromosomes 3 and 10.

Serero S, Maire P, Nguyen VC, Cohen-Haguenauer O, Gross MS, Jégou-Foubert C, de Tand MF, Kahn A, Frézal J. Serero S, et al. Hum Genet. 1988 Feb;78(2):167-74. doi: 10.1007/BF00278190. Hum Genet. 1988. PMID: 2828224

10

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

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