McElreavey K - Search Results

1

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: mcelreavey k. C R Acad Sci III. 1993;316(4):375-83. C R Acad Sci III. 1993. PMID: 8402263

2

The sole presence of the testis-determining region of the Y chromosome (SRY) in 46,XX patients is associated with phenotypic variability.

Boucekkine C, Toublanc JE, Abbas N, Semrouni M, Vilain E, McElreavey K, Mugneret F, Fellous M. Boucekkine C, et al. Among authors: mcelreavey k. Horm Res. 1992;37(6):236-40. doi: 10.1159/000182319. Horm Res. 1992. PMID: 1292977

3

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

4

[Isolation of the sex-determining gene in men].

Vilain E, McElreavey K, Richaud F, Fellous M. Vilain E, et al. Among authors: mcelreavey k. Pathol Biol (Paris). 1992 Jan;40(1):15-7. Pathol Biol (Paris). 1992. PMID: 1570176 Review. French. No abstract available.

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

6

XY sex reversal associated with a nonsense mutation in SRY.

McElreavey KD, Vilain E, Boucekkine C, Vidaud M, Jaubert F, Richaud F, Fellous M. McElreavey KD, et al. Genomics. 1992 Jul;13(3):838-40. doi: 10.1016/0888-7543(92)90164-n. Genomics. 1992. PMID: 1639410

7

[The analysis of SRY doesn't explain all the pathology of sex determination].

Vilain E, McElreavey K, Vidaud M, Richaud F, Fellous M. Vilain E, et al. Among authors: mcelreavey k. Ann Endocrinol (Paris). 1991;52(6):435-6. Ann Endocrinol (Paris). 1991. PMID: 1824496 French. No abstract available.

8

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

9

SRY-negative XX fetus with complete male phenotype.

Vilain E, Le Fiblec B, Morichon-Delvallez N, Brauner R, Dommergues M, Dumez Y, Jaubert F, Boucekkine C, McElreavey K, Vekemans M, et al. Vilain E, et al. Among authors: mcelreavey k. Lancet. 1994 Jan 22;343(8891):240-1. doi: 10.1016/s0140-6736(94)91029-4. Lancet. 1994. PMID: 7904700 No abstract available.

10

Gonadal agenesis in XX and XY sisters: evidence for the involvement of an autosomal gene.

Mendonça BB, Barbosa AS, Arnhold IJ, McElreavey K, Fellous M, Moreira-Filho CA. Mendonça BB, et al. Among authors: mcelreavey k. Am J Med Genet. 1994 Aug 1;52(1):39-43. doi: 10.1002/ajmg.1320520108. Am J Med Genet. 1994. PMID: 7977459

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