Brauch H - Search Results

1

Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central Europe.

Glavac D, Neumann HP, Wittke C, Jaenig H, Masek O, Streicher T, Pausch F, Engelhardt D, Plate KH, Höfler H, Chen F, Zbar B, Brauch H. Glavac D, et al. Among authors: brauch h. Hum Genet. 1996 Sep;98(3):271-80. doi: 10.1007/s004390050206. Hum Genet. 1996. PMID: 8707293

2

Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes.

Lerman MI, Latif F, Glenn GM, Daniel LN, Brauch H, Hosoe S, Hampsch K, Delisio J, Orcutt ML, McBride OW, et al. Lerman MI, et al. Among authors: brauch h. Hum Genet. 1991 Apr;86(6):567-77. doi: 10.1007/BF00201543. Hum Genet. 1991. PMID: 1673958

3

A new polymorphic probe on chromosome 3p: lambda LIB45-82 (D3S232).

Latif F, Glenn GM, Daniel LN, Brauch H, Delisio J, Hampsch K, Orcutt ML, Zbar B, Lerman MI. Latif F, et al. Among authors: brauch h. Nucleic Acids Res. 1990 Mar 25;18(6):1662. doi: 10.1093/nar/18.6.1662-a. Nucleic Acids Res. 1990. PMID: 1691487 Free PMC article. No abstract available.

4

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma.

Zbar B, Brauch H, Talmadge C, Linehan M. Zbar B, et al. Among authors: brauch h. Nature. 1987 Jun 25-Jul 1;327(6124):721-4. doi: 10.1038/327721a0. Nature. 1987. PMID: 2885753

5

[Hippel-Lindau syndrome and sporadic renal cell carcinomas. Pathogenesis, morphologic spectrum and molecular genetics].

Brauch H, Böhm J, Höfler H. Brauch H, et al. Pathologe. 1995 Sep;16(5):321-7. doi: 10.1007/s002920050109. Pathologe. 1995. PMID: 7479604 Review. German.

6

[Molecular diagnosis of the Hippel-Lindau syndrome].

Neumann HP, Brauch H. Neumann HP, et al. Among authors: brauch h. Dtsch Med Wochenschr. 1995 Oct 13;120(41):1416. Dtsch Med Wochenschr. 1995. PMID: 7555669 German. No abstract available.

7

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.

Neumann HP, Eng C, Mulligan LM, Glavac D, Zäuner I, Ponder BA, Crossey PA, Maher ER, Brauch H. Neumann HP, et al. Among authors: brauch h. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

8

Microsatellite instability in adenocarcinomas of the upper gastrointestinal tract. Relation to clinicopathological data and family history.

Keller G, Rotter M, Vogelsang H, Bischoff P, Becker KF, Mueller J, Brauch H, Siewert JR, Höfler H. Keller G, et al. Among authors: brauch h. Am J Pathol. 1995 Sep;147(3):593-600. Am J Pathol. 1995. PMID: 7677173 Free PMC article.

9

Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect.

Brauch H, Kishida T, Glavac D, Chen F, Pausch F, Höfler H, Latif F, Lerman MI, Zbar B, Neumann HP. Brauch H, et al. Hum Genet. 1995 May;95(5):551-6. doi: 10.1007/BF00223868. Hum Genet. 1995. PMID: 7759077

10

Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGH.

Decker HJ, Neuhaus C, Jauch A, Speicher M, Ried T, Bujard M, Brauch H, Störkel S, Stöckle M, Seliger B, Huber C. Decker HJ, et al. Among authors: brauch h. Hum Genet. 1996 Jun;97(6):770-6. doi: 10.1007/BF02346188. Hum Genet. 1996. PMID: 8641695

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