Siffroi JP - Search Results

1

Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature.

Heide S, Afenjar A, Edery P, Sanlaville D, Keren B, Rouen A, Lavillaureix A, Hyon C, Doummar D, Siffroi JP, Chantot-Bastaraud S. Heide S, et al. Among authors: siffroi jp. Eur J Med Genet. 2015 Jun-Jul;58(6-7):341-5. doi: 10.1016/j.ejmg.2015.04.003. Epub 2015 Apr 23. Eur J Med Genet. 2015. PMID: 25917374 Review.

2

Prenatal diagnosis of a large centromeric heteromorphism of chromosome 12: implications for genetic counseling.

Chantot-Bastaraud S, Siffroi JP, Berkane N, Heim N, Herve F, Uzan S, Vendrely E. Chantot-Bastaraud S, et al. Among authors: siffroi jp. Fetal Diagn Ther. 2003 Mar-Apr;18(2):111-3. doi: 10.1159/000068071. Fetal Diagn Ther. 2003. PMID: 12576746

3

Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.

Chantot-Bastaraud S, Muti C, Pipiras E, Routon MC, Roubergue A, Burglen L, Siffroi JP, Simon-Bouy B. Chantot-Bastaraud S, et al. Among authors: siffroi jp. Ann Genet. 2004 Jul-Sep;47(3):241-9. doi: 10.1016/j.anngen.2004.02.003. Ann Genet. 2004. PMID: 15337469 Review.

4

GR/GR deletions within the azoospermia factor c region on the Y chromosome might not be associated with spermatogenic failure.

Ravel C, Chantot-Bastaraud S, El Houate B, Mandelbaum J, Siffroi JP, McElreavey K. Ravel C, et al. Among authors: siffroi jp. Fertil Steril. 2006 Jan;85(1):229-31. doi: 10.1016/j.fertnstert.2005.07.1278. Fertil Steril. 2006. PMID: 16412764 Free article.

5

Y chromosome variants and male reproductive function.

McElreavey K, Ravel C, Chantot-Bastaraud S, Siffroi JP. McElreavey K, et al. Among authors: siffroi jp. Int J Androl. 2006 Feb;29(1):298-303; discussion 304-6. doi: 10.1111/j.1365-2605.2005.00637.x. Int J Androl. 2006. PMID: 16466551 Review.

6

Tail stump syndrome associated with chromosomal translocation in two brothers attempting intracytoplasmic sperm injection.

Ravel C, Chantot-Bastaraud S, Siffroi JP, Escalier D, Antoine JM, Mandelbaum J. Ravel C, et al. Among authors: siffroi jp. Fertil Steril. 2006 Sep;86(3):719.e1-7. doi: 10.1016/j.fertnstert.2005.12.078. Fertil Steril. 2006. PMID: 16952512 Free article.

7

[Y chromosome and male infertility: what is a normal Y chromosome?].

McElreavey K, Chantot-Bastaraud S, Ravel C, Mandelbaum J, Siffroi JP. McElreavey K, et al. Among authors: siffroi jp. J Soc Biol. 2008;202(2):135-41. doi: 10.1051/jbio:2008017. Epub 2008 Jun 13. J Soc Biol. 2008. PMID: 18547511 French.

8

Y-chromosome AZFc structural architecture and relationship to male fertility.

Ravel C, Chantot-Bastaraud S, El Houate B, Rouba H, Legendre M, Lorenço D, Mandelbaum J, Siffroi JP, McElreavey K. Ravel C, et al. Among authors: siffroi jp. Fertil Steril. 2009 Dec;92(6):1924-33. doi: 10.1016/j.fertnstert.2008.08.135. Epub 2008 Nov 6. Fertil Steril. 2009. PMID: 18990391 Free article.

9

Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.

Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C. Depienne C, et al. Among authors: siffroi jp. Biol Psychiatry. 2009 Aug 15;66(4):349-59. doi: 10.1016/j.biopsych.2009.01.025. Epub 2009 Mar 17. Biol Psychiatry. 2009. PMID: 19278672 Free article.

10

Atypical deletion of 22q11.2: detection using the FISH TBX1 probe and molecular characterization with high-density SNP arrays.

Beaujard MP, Chantot S, Dubois M, Keren B, Carpentier W, Mabboux P, Whalen S, Vodovar M, Siffroi JP, Portnoï MF. Beaujard MP, et al. Among authors: siffroi jp. Eur J Med Genet. 2009 Sep-Oct;52(5):321-7. doi: 10.1016/j.ejmg.2009.05.010. Epub 2009 May 23. Eur J Med Genet. 2009. PMID: 19467348

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