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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1979 | 1 |
1987 | 1 |
1989 | 1 |
1997 | 1 |
1999 | 1 |
2000 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 98015
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Genetic homogeneity of the urofacial (Ochoa) syndrome confirmed in a new French family.
Am J Med Genet. 2000 Nov 6;95(1):10-2. doi: 10.1002/1096-8628(20001106)95:1<10::aid-ajmg3>3.0.co;2-z.
Am J Med Genet. 2000.
PMID: 11074487
Genetic homogeneity, high-resolution mapping, and mutation analysis of the urofacial (Ochoa) syndrome and exclusion of the glutamate oxaloacetate transaminase gene (GOT1) in the critical region as the disease gene.
Wang CY, Huang YQ, Shi JD, Marron MP, Ruan QG, Hawkins-Lee B, Ochoa B, She JX.
Wang CY, et al.
Am J Med Genet. 1999 Jun 11;84(5):454-9.
Am J Med Genet. 1999.
PMID: 10360399
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Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24.
Wang CY, Hawkins-Lee B, Ochoa B, Walker RD, She JX.
Wang CY, et al.
Am J Hum Genet. 1997 Jun;60(6):1461-7. doi: 10.1086/515469.
Am J Hum Genet. 1997.
PMID: 9199567
Free PMC article.
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Urofacial (ochoa) syndrome.
Ochoa B, Gorlin RJ.
Ochoa B, et al.
Am J Med Genet. 1987 Jul;27(3):661-7. doi: 10.1002/ajmg.1320270320.
Am J Med Genet. 1987.
PMID: 3631137
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Urofacial syndrome.
Teebi AS, Farag TI, el-Khalifa MY, Besisso MS, al-Ansari AG.
Teebi AS, et al.
Am J Med Genet. 1989 Dec;34(4):608. doi: 10.1002/ajmg.1320340432.
Am J Med Genet. 1989.
PMID: 2624278
No abstract available.
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Genetic and diagnostic considerations in three families with abnormalities of facial expression and congenital urinary obstruction: "The Ochoa syndrome".
Elejalde BR.
Elejalde BR.
Am J Med Genet. 1979;3(1):97-108. doi: 10.1002/ajmg.1320030114.
Am J Med Genet. 1979.
PMID: 474623
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