Barbaux S - Search Results

1

Ullrich-Turner syndrome: relevance of searching for Y chromosome fragments.

Damiani D, Guedes DR, Fellous M, Barbaux S, McElreavey K, Kalil J, Goldberg AC, Moreira-Filho CA, Barbosa A, Della Manna T, Dichtchekenian V, Setian N. Damiani D, et al. Among authors: barbaux s. J Pediatr Endocrinol Metab. 1999 Nov-Dec;12(6):827-31. doi: 10.1515/jpem.1999.12.6.827. J Pediatr Endocrinol Metab. 1999. PMID: 10614539

2

True hermaphroditism: clinical aspects and molecular studies in 16 cases.

Damiani D, Fellous M, McElreavey K, Barbaux S, Barreto ES, Dichtchekenian V, Setian N. Damiani D, et al. Among authors: barbaux s. Eur J Endocrinol. 1997 Feb;136(2):201-4. doi: 10.1530/eje.0.1360201. Eur J Endocrinol. 1997. PMID: 9116916

3

Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata.

Barbaux S, Vilain E, Raoul O, Gilgenkrantz S, Jeandidier E, Chadenas D, Souleyreau N, Fellous M, McElreavey K. Barbaux S, et al. Hum Mol Genet. 1995 Sep;4(9):1565-8. doi: 10.1093/hmg/4.9.1565. Hum Mol Genet. 1995. PMID: 8541840

4

Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype.

Veitia R, Ion A, Barbaux S, Jobling MA, Souleyreau N, Ennis K, Ostrer H, Tosi M, Meo T, Chibani J, Fellous M, McElreavey K. Veitia R, et al. Among authors: barbaux s. Hum Genet. 1997 May;99(5):648-52. doi: 10.1007/s004390050422. Hum Genet. 1997. PMID: 9150734

5

[46,XX karyotype males, based on a specific case].

Tar A, Rácz K, Dobos M, Barbaux S, McElreavey K, Fellous M. Tar A, et al. Among authors: barbaux s. Orv Hetil. 1996 May 19;137(20):1085-7. Orv Hetil. 1996. PMID: 8657421 Hungarian.

6

Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion.

Tar A, Sólyom J, Györvári B, Ion A, Telvi L, Barbaux S, Souleyreau N, Vilain E, Fellous M, McElreavey K. Tar A, et al. Among authors: barbaux s. Hum Genet. 1995 Oct;96(4):464-8. doi: 10.1007/BF00191807. Hum Genet. 1995. PMID: 7557971

7

[Y chromosome and spermatogenesis].

Bourgeron T, Barbaux S, McElreavey K, Fellous M. Bourgeron T, et al. Among authors: barbaux s. Contracept Fertil Sex. 1997 Jul-Aug;25(7-8):620-5. Contracept Fertil Sex. 1997. PMID: 9410377 Review. French.

8

Sex chromosome mosaicism in males carrying Y chromosome long arm deletions.

Siffroi JP, Le Bourhis C, Krausz C, Barbaux S, Quintana-Murci L, Kanafani S, Rouba H, Bujan L, Bourrouillou G, Seifer I, Boucher D, Fellous M, McElreavey K, Dadoune JP. Siffroi JP, et al. Among authors: barbaux s. Hum Reprod. 2000 Dec;15(12):2559-62. doi: 10.1093/humrep/15.12.2559. Hum Reprod. 2000. PMID: 11098026

9

Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13.

Tar A, Ion A, Sólyom J, Györvári B, Stephenson C, Barbaux S, Nunes M, Fellous M, McElreavey K. Tar A, et al. Among authors: barbaux s. Am J Med Genet. 1997 Jan 20;68(2):231-5. doi: 10.1002/(sici)1096-8628(19970120)68:2<231::aid-ajmg22>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9028465

10

A high frequency of Y chromosome deletions in males with nonidiopathic infertility.

Krausz C, Quintana-Murci L, Barbaux S, Siffroi JP, Rouba H, Delafontaine D, Souleyreau-Therville N, Arvis G, Antoine JM, Erdei E, Taar JP, Tar A, Jeandidier E, Plessis G, Bourgeron T, Dadoune JP, Fellous M, McElreavey K. Krausz C, et al. Among authors: barbaux s. J Clin Endocrinol Metab. 1999 Oct;84(10):3606-12. doi: 10.1210/jcem.84.10.6040. J Clin Endocrinol Metab. 1999. PMID: 10523003

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