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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1990 | 1 |
1992 | 3 |
1998 | 1 |
2024 | 0 |
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5 results
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Page 1
Independent observation of SRY mutation I90M in a patient with complete gonadal dysgenesis.
Hum Mutat. 1998;11(1):90-1. doi: 10.1002/(SICI)1098-1004(1998)11:1<90::AID-HUMU14>3.0.CO;2-U.
Hum Mutat. 1998.
PMID: 9450909
No abstract available.
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.
Am J Hum Genet. 1992 May;50(5):1008-11.
Am J Hum Genet. 1992.
PMID: 1570829
Free PMC article.
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Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis.
Hawkins JR, Taylor A, Goodfellow PN, Migeon CJ, Smith KD, Berkovitz GD.
Hawkins JR, et al.
Am J Hum Genet. 1992 Nov;51(5):979-84.
Am J Hum Genet. 1992.
PMID: 1415266
Free PMC article.
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Genetic evidence equating SRY and the testis-determining factor.
Berta P, Hawkins JR, Sinclair AH, Taylor A, Griffiths BL, Goodfellow PN, Fellous M.
Berta P, et al.
Nature. 1990 Nov 29;348(6300):448-50. doi: 10.1038/348448A0.
Nature. 1990.
PMID: 2247149
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A familial mutation in the testis-determining gene SRY shared by both sexes.
Jäger RJ, Harley VR, Pfeiffer RA, Goodfellow PN, Scherer G.
Jäger RJ, et al.
Hum Genet. 1992 Dec;90(4):350-5. doi: 10.1007/BF00220457.
Hum Genet. 1992.
PMID: 1483689
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