Schmidt LS - Search Results

1

BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports.

Toro JR, Wei MH, Glenn GM, Weinreich M, Toure O, Vocke C, Turner M, Choyke P, Merino MJ, Pinto PA, Steinberg SM, Schmidt LS, Linehan WM. Toro JR, et al. Among authors: schmidt ls. J Med Genet. 2008 Jun;45(6):321-31. doi: 10.1136/jmg.2007.054304. Epub 2008 Jan 30. J Med Genet. 2008. PMID: 18234728 Free PMC article. Review.

2

A microsatellite polymorphic probe on chromosome 3p: lambda LIB12-2CATT (D3S1244).

Li H, Kalman T, Duh FM, Schmidt L, Wei MH, Lerman MI, Zbar B. Li H, et al. Hum Mol Genet. 1992 Sep;1(6):452. doi: 10.1093/hmg/1.6.452-a. Hum Mol Genet. 1992. PMID: 1301919 No abstract available.

3

Molecular and genetic characterization and physical mapping of 11 new markers detecting multiallele restriction fragment length polymorphisms on the short arm of human chromosome 3.

Latif F, Modi WS, Duh FM, Schmidt L, Li H, Geil L, Orcutt ML, Heppell-Parton A, Rabbitts PH, Linehan WM, et al. Latif F, et al. Hum Genet. 1992 Sep-Oct;90(1-2):17-22. doi: 10.1007/BF00210739. Hum Genet. 1992. PMID: 1358787

4

A new polymorphic probe on chromosome 3p:lambda LIB4A-52''(D3S732).

Latif F, Glenn GM, Geil L, Schmidt L, Delisio J, Hampsch K, Orcutt ML, Zbar B, Lerman MI. Latif F, et al. Nucleic Acids Res. 1991 May 25;19(10):2802. doi: 10.1093/nar/19.10.2802. Nucleic Acids Res. 1991. PMID: 1674995 Free PMC article. No abstract available.

5

Mutations of the VHL tumour suppressor gene in renal carcinoma.

Gnarra JR, Tory K, Weng Y, Schmidt L, Wei MH, Li H, Latif F, Liu S, Chen F, Duh FM, et al. Gnarra JR, et al. Nat Genet. 1994 May;7(1):85-90. doi: 10.1038/ng0594-85. Nat Genet. 1994. PMID: 7915601

6

A microsatellite, D8S602, adjacent to the MSR gene.

Schmidt L, Pozzatti R, Li H, Wei MH, Vocke C, Linehan WM, Tory K. Schmidt L, et al. Hum Mol Genet. 1994 Apr;3(4):679. doi: 10.1093/hmg/3.4.679. Hum Mol Genet. 1994. PMID: 8069323 No abstract available.

7

Fourteen new polymorphic dinucleotide repeats on human chromosome 3: D3S1432, D3S1433, D3S1434, D3S1483, D3S1484, D3S1485, D3S1486, D3S1487, D3S1488, D3S1489, D3S1490, D3S1496, D3S1497 and D3S1498.

Li H, Schmidt L, Wei MH, Hustad T, Lerman MI, Zbar B, Tory K. Li H, et al. Hum Mol Genet. 1994 May;3(5):837. doi: 10.1093/hmg/3.5.837. Hum Mol Genet. 1994. PMID: 8081375 No abstract available.

8

A polymorphic dinucleotide repeat probe on chromosome 3p: LIB 44-36ca (D3S769).

Schmidt L, Li H, Wei MH, Lerman MI, Zbar B, Tory K. Schmidt L, et al. Hum Mol Genet. 1993 Jan;2(1):89. doi: 10.1093/hmg/2.1.89-a. Hum Mol Genet. 1993. PMID: 8098247 No abstract available.

9

Hereditary papillary renal cell carcinoma.

Zbar B, Tory K, Merino M, Schmidt L, Glenn G, Choyke P, Walther MM, Lerman M, Linehan WM. Zbar B, et al. J Urol. 1994 Mar;151(3):561-6. doi: 10.1016/s0022-5347(17)35015-2. J Urol. 1994. PMID: 8308957 Review.

10

Six dinucleotide microsatellite polymorphisms on human chromosome 3.

Schmidt L, Li H, Wei MH, Lerman MI, Zbar B, Tory K. Schmidt L, et al. Hum Mol Genet. 1993 Jun;2(6):817-8. doi: 10.1093/hmg/2.6.817. Hum Mol Genet. 1993. PMID: 8353502 No abstract available.

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