Fellous M - Search Results

1

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. Among authors: fellous m. Hum Mol Genet. 1995 Sep;4(9):1565-8. doi: 10.1093/hmg/4.9.1565. Hum Mol Genet. 1995. PMID: 8541840

2

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: fellous m. Hum Genet. 1997 May;99(5):648-52. doi: 10.1007/s004390050422. Hum Genet. 1997. PMID: 9150734

3

[Y chromosome and spermatogenesis].

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

4

Sex determination and the Y chromosome.

McElreavey K, Fellous M. McElreavey K, et al. Among authors: fellous m. Am J Med Genet. 1999 Dec 29;89(4):176-85. doi: 10.1002/(sici)1096-8628(19991229)89:4<176::aid-ajmg2>3.0.co;2-b. Am J Med Genet. 1999. PMID: 10727993 Review.

5

Familial case with sequence variant in the testis-determining region associated with two sex phenotypes.

Vilain E, McElreavey K, Jaubert F, Raymond JP, Richaud F, Fellous M. Vilain E, et al. Among authors: fellous m. Am J Hum Genet. 1992 May;50(5):1008-11. Am J Hum Genet. 1992. PMID: 1570829 Free PMC article.

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: fellous m. Hum Genet. 1995 Oct;96(4):464-8. doi: 10.1007/BF00191807. Hum Genet. 1995. PMID: 7557971

7

Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.

Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M. Abbas N, et al. Among authors: fellous m. C R Acad Sci III. 1993;316(4):375-83. C R Acad Sci III. 1993. PMID: 8402263

8

Pathology of 46,XY pure gonadal dysgenesis: absence of testis differentiation associated with mutations in the testis-determining factor.

Vilain E, Jaubert F, Fellous M, McElreavey K. Vilain E, et al. Among authors: fellous m. Differentiation. 1993 Jan;52(2):151-9. doi: 10.1111/j.1432-0436.1993.tb00625.x. Differentiation. 1993. PMID: 8472885

9

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: fellous m. Heredity (Edinb). 1995 Dec;75 ( Pt 6):599-611. doi: 10.1038/hdy.1995.179. Heredity (Edinb). 1995. PMID: 8575930 Review.

10

A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome.

Ion A, Telvi L, Chaussain JL, Galacteros F, Valayer J, Fellous M, McElreavey K. Ion A, et al. Among authors: fellous m. Am J Hum Genet. 1996 Jun;58(6):1185-91. Am J Hum Genet. 1996. PMID: 8651295 Free PMC article.

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