McElreavey K - Search Results

1

Y-chromosome lineages trace diffusion of people and languages in southwestern Asia.

Quintana-Murci L, Krausz C, Zerjal T, Sayar SH, Hammer MF, Mehdi SQ, Ayub Q, Qamar R, Mohyuddin A, Radhakrishna U, Jobling MA, Tyler-Smith C, McElreavey K. Quintana-Murci L, et al. Among authors: mcelreavey k. Am J Hum Genet. 2001 Feb;68(2):537-42. doi: 10.1086/318200. Epub 2000 Dec 27. Am J Hum Genet. 2001. PMID: 11133362 Free PMC article.

2

A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY.

McElreavey K, Rappaport R, Vilain E, Abbas N, Richaud F, Lortat-Jacob S, Berger R, Le Coniat M, Boucekkine C, Kucheria K, et al. McElreavey K, et al. Hum Genet. 1992 Sep-Oct;90(1-2):121-5. doi: 10.1007/BF00210754. Hum Genet. 1992. PMID: 1427767

3

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: mcelreavey k. Am J Hum Genet. 1992 May;50(5):1008-11. Am J Hum Genet. 1992. PMID: 1570829 Free PMC article.

4

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: mcelreavey k. Hum Mol Genet. 1995 Sep;4(9):1565-8. doi: 10.1093/hmg/4.9.1565. Hum Mol Genet. 1995. PMID: 8541840

5

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

6

Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome.

Veitia RA, Nunes M, Quintana-Murci L, Rappaport R, Thibaud E, Jaubert F, Fellous M, McElreavey K, Gonçalves J, Silva M, Rodrigues JC, Caspurro M, Boieiro F, Marques R, Lavinha J. Veitia RA, et al. Among authors: mcelreavey k. Am J Hum Genet. 1998 Sep;63(3):901-5. doi: 10.1086/302023. Am J Hum Genet. 1998. PMID: 9718353 Free PMC article. No abstract available.

7

The INSL4 gene maps close to WI-5527 at 9p24.1-->p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome.

Veitia R, Laurent A, Quintana-Murci L, Ottolenghi C, Fellous M, Vidaud M, McElreavey K. Veitia R, et al. Among authors: mcelreavey k. Cytogenet Cell Genet. 1998;81(3-4):275-7. doi: 10.1159/000015045. Cytogenet Cell Genet. 1998. PMID: 9730618

8

Y chromosome and male infertility.

Krausz C, McElreavey K. Krausz C, et al. Among authors: mcelreavey k. Front Biosci. 1999 Jan 15;4:E1-8. doi: 10.2741/krausz. Front Biosci. 1999. PMID: 9889182 Review.

9

Sex Chromosome Genetics '99. Male infertility and the Y chromosome.

McElreavey K, Krausz C. McElreavey K, et al. Am J Hum Genet. 1999 Apr;64(4):928-33. doi: 10.1086/302351. Am J Hum Genet. 1999. PMID: 10090876 Free PMC article. Review. No abstract available.

10

[Genetic control of spermatogenesis: Y chromosome and male infertility].

Krausz C, Siffroi J, Souleyreau-Therville N, Bourgeron T, McElreavey K, Fellous M. Krausz C, et al. Among authors: mcelreavey k. Ann Biol Clin (Paris). 1999 May;57(3):309-17. Ann Biol Clin (Paris). 1999. PMID: 10377481 Free article. Review. French. No abstract available.

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