Barbaux S - Search Results

1

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD. McElreavey K, et al. Among authors: barbaux s. Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8590-4. doi: 10.1073/pnas.93.16.8590. Proc Natl Acad Sci U S A. 1996. PMID: 8710915 Free PMC article.

2

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

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

The genetic basis of murine and human sex determination: a review.

McElreavey K, Barbaux S, Ion A, Fellous M. McElreavey K, et al. Among authors: barbaux s. Heredity (Edinb). 1995 Dec;75 ( Pt 6):599-611. doi: 10.1038/hdy.1995.179. Heredity (Edinb). 1995. PMID: 8575930 Review.

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

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

7

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

8

Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene.

Seboun E, Barbaux S, Bourgeron T, Nishi S, Agulnik A, Egashira M, Nikkawa N, Bishop C, Fellous M, McElreavey K, Kasahara M. Seboun E, et al. Among authors: barbaux s. Genomics. 1997 Apr 15;41(2):227-35. doi: 10.1006/geno.1997.4635. Genomics. 1997. PMID: 9143498

9

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

10

[Could male infertility become hereditary?].

Barbaux S, Fellous M. Barbaux S, et al. Contracept Fertil Sex. 1997 Mar;25(3):192-3. Contracept Fertil Sex. 1997. PMID: 9156705 French. No abstract available.

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