Clement P - Search Results

1

First prenatal diagnosis of a 'pure' 9q34.3 deletion (Kleefstra syndrome): A case report and literature review.

Guterman S, Hervé B, Rivière J, Fauvert D, Clement P, Vialard F. Guterman S, et al. Among authors: clement p. J Obstet Gynaecol Res. 2018 Mar;44(3):570-575. doi: 10.1111/jog.13517. Epub 2017 Nov 21. J Obstet Gynaecol Res. 2018. PMID: 29160022 Review.

2

Sperm chromosome analysis in two cases of paracentric inversion.

Vialard F, Delanete A, Clement P, Simon-Bouy B, Aubriot FX, Selva J. Vialard F, et al. Among authors: clement p. Fertil Steril. 2007 Feb;87(2):418.e1-5. doi: 10.1016/j.fertnstert.2006.05.087. Epub 2006 Nov 27. Fertil Steril. 2007. PMID: 17126336 Free article.

3

Is classic pericentric inversion of chromosome 2 inv(2)(p11q13) associated with an increased risk of unbalanced chromosomes?

Ferfouri F, Clement P, Gomes DM, Minz M, Amar E, Selva J, Vialard F. Ferfouri F, et al. Among authors: clement p. Fertil Steril. 2009 Oct;92(4):1497.e1-1497.e4. doi: 10.1016/j.fertnstert.2009.06.047. Epub 2009 Aug 8. Fertil Steril. 2009. PMID: 19665704 Free article.

4

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: clement p. Prenat Diagn. 2011 May;31(5):500-8. doi: 10.1002/pd.2727. Epub 2011 Mar 14. Prenat Diagn. 2011. PMID: 21404304

5

The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type.

Ferfouri F, Selva J, Boitrelle F, Gomes DM, Torre A, Albert M, Bailly M, Clement P, Vialard F. Ferfouri F, et al. Among authors: clement p. Fertil Steril. 2011 Dec;96(6):1337-43. doi: 10.1016/j.fertnstert.2011.09.008. Epub 2011 Oct 1. Fertil Steril. 2011. PMID: 21963229 Free article.

6

Can one translocation impact the meiotic segregation of another translocation? A sperm-FISH analysis of a 46,XY,t(1;16)(q21;p11.2),t(8;9) (q24.3;p24) patient and his 46,XY,t(8;9)(q24.3;p24) brother and cousin.

Ferfouri F, Boitrelle F, Clément P, Molina Gomes D, Selva J, Vialard F. Ferfouri F, et al. Among authors: clement p. Mol Hum Reprod. 2013 Feb;19(2):109-17. doi: 10.1093/molehr/gas048. Epub 2012 Oct 25. Mol Hum Reprod. 2013. PMID: 23100463

7

Sperm FISH analysis of a 44,X,der(Y),t(Y;15)(q12;q10)pat,rob(13;14)(q10;q10)mat complex chromosome rearrangement.

Ferfouri F, Boitrelle F, Clement P, Molina Gomes D, Selva J, Vialard F. Ferfouri F, et al. Among authors: clement p. Andrologia. 2014 Jun;46(5):576-82. doi: 10.1111/and.12112. Epub 2013 May 22. Andrologia. 2014. PMID: 23701584

8

Evidence for high breakpoint variability in 46, XX, SRY-positive testicular disorder and frequent ARSE deletion that may be associated with short stature.

Capron C, Januel L, Vieville G, Jaillard S, Kuentz P, Salaun G, Nadeau G, Clement P, Brechard MP, Herve B, Dupont JM, Gruchy N, Chambon P, Abdelhedi F, Dahlen E, Vago P, Harbuz R, Plotton I, Coutton C, Belaud-Rotureau MA, Schluth-Bolard C, Vialard F. Capron C, et al. Among authors: clement p. Andrology. 2022 Nov;10(8):1625-1631. doi: 10.1111/andr.13279. Epub 2022 Sep 7. Andrology. 2022. PMID: 36026611 Free article.

9

A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45,X Cell Line: (46,X,psu dic(X;Y)(p22.13;q11.221)/45,X/45,psu dic(X;Y)(p22.13;q11.221).

Clement A, Dominot T, Chammas J, Montagnon M, Delcroix M, Pfeffer J, Dupont JM, Lebbar A, Clement P, Vialard F. Clement A, et al. Among authors: clement p. Genes (Basel). 2022 Dec 27;14(1):81. doi: 10.3390/genes14010081. Genes (Basel). 2022. PMID: 36672822 Free PMC article.

10

[Screening for Y chromosome microdeletions in assisted reproductive techniques].

Clément P, Lohmann L, Minz M. Clément P, et al. Gynecol Obstet Fertil. 2008 Mar;36(3):318-24. doi: 10.1016/j.gyobfe.2007.12.015. Epub 2008 Mar 12. Gynecol Obstet Fertil. 2008. PMID: 18339572 French.

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