Klinger K - Search Results

1

Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.

Dixon MJ, Dixon J, Houseal T, Bhatt M, Ward DC, Klinger K, Landes GM. Dixon MJ, et al. Among authors: klinger k. Am J Hum Genet. 1993 May;52(5):907-14. Am J Hum Genet. 1993. PMID: 8488840 Free PMC article.

2

Loss of GM3 synthase gene, but not sphingosine kinase 1, is protective against murine nephronophthisis-related polycystic kidney disease.

Natoli TA, Husson H, Rogers KA, Smith LA, Wang B, Budman Y, Bukanov NO, Ledbetter SR, Klinger KW, Leonard JP, Ibraghimov-Beskrovnaya O. Natoli TA, et al. Hum Mol Genet. 2012 Aug 1;21(15):3397-407. doi: 10.1093/hmg/dds172. Epub 2012 May 4. Hum Mol Genet. 2012. PMID: 22563011 Free PMC article.

3

What's in a spot?

Houseal TW, Klinger KW. Houseal TW, et al. Among authors: klinger kw. Hum Mol Genet. 1994 Aug;3(8):1215-6. doi: 10.1093/hmg/3.8.1215. Hum Mol Genet. 1994. PMID: 7987294 No abstract available.

4

High throughput parallel analysis of hundreds of patient samples for more than 100 mutations in multiple disease genes.

Shuber AP, Michalowsky LA, Nass GS, Skoletsky J, Hire LM, Kotsopoulos SK, Phipps MF, Barberio DM, Klinger KW. Shuber AP, et al. Among authors: klinger kw. Hum Mol Genet. 1997 Mar;6(3):337-47. doi: 10.1093/hmg/6.3.337. Hum Mol Genet. 1997. PMID: 9147636

5

Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH).

Klinger K, Landes G, Shook D, Harvey R, Lopez L, Locke P, Lerner T, Osathanondh R, Leverone B, Houseal T, et al. Klinger K, et al. Am J Hum Genet. 1992 Jul;51(1):55-65. Am J Hum Genet. 1992. PMID: 1609805 Free PMC article.

6

Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2.

Dixon MJ, Dixon J, Raskova D, Le Beau MM, Williamson R, Klinger K, Landes GM. Dixon MJ, et al. Among authors: klinger k. Hum Mol Genet. 1992 Jul;1(4):249-53. doi: 10.1093/hmg/1.4.249. Hum Mol Genet. 1992. PMID: 1303194

7

Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells.

Ried T, Landes G, Dackowski W, Klinger K, Ward DC. Ried T, et al. Among authors: klinger k. Hum Mol Genet. 1992 Aug;1(5):307-13. doi: 10.1093/hmg/1.5.307. Hum Mol Genet. 1992. PMID: 1303206

8

Maternal origin of nucleated erythrocytes in peripheral venous blood of pregnant women.

Slunga-Tallberg A, el-Rifai W, Keinänen M, Ylinen K, Kurki T, Klinger K, Ylikorkala O, Knuutila S. Slunga-Tallberg A, et al. Among authors: klinger k. Hum Genet. 1995 Jul;96(1):53-7. doi: 10.1007/BF00214186. Hum Genet. 1995. PMID: 7607654

9

Cystic fibrosis mutations in the Hutterite Brethren.

Klinger K, Horn GT, Stanislovitis P, Schwartz RH, Fujiwara TM, Morgan K. Klinger K, et al. Am J Hum Genet. 1990 May;46(5):983-7. Am J Hum Genet. 1990. PMID: 2339696 Free PMC article.

10

Further data on linkage between cystic fibrosis and 7C22 (D7S16).

Farrall M, Lathrop M, Spence JE, Bowcock A, Klinger K, Tsui LC. Farrall M, et al. Among authors: klinger k. Am J Hum Genet. 1987 Aug;41(2):286-7. Am J Hum Genet. 1987. PMID: 3475980 Free PMC article. No abstract available.

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