Tantravahi U - Search Results

1

Regional localization of 32 NotI-HindIII fragments from a human chromosome 13 library by a somatic cell hybrid panel and in situ hybridization.

Warburton D, Yu MT, Tantravahi U, Lee C, Cayanis E, Russo J, Fischer SG. Warburton D, et al. Among authors: tantravahi u. Genomics. 1993 May;16(2):355-60. doi: 10.1006/geno.1993.1197. Genomics. 1993. PMID: 8314575 Free article.

2

A microsatellite genetic linkage map of human chromosome 13.

Petrukhin KE, Speer MC, Cayanis E, Bonaldo MF, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J. Petrukhin KE, et al. Among authors: tantravahi u. Genomics. 1993 Jan;15(1):76-85. doi: 10.1006/geno.1993.1012. Genomics. 1993. PMID: 8432553

3

Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathy.

Bonilla E, Younger DS, Chang HW, Tantravahi U, Miranda AF, Medori R, DiMauro S, Warburton D, Rowland LP. Bonilla E, et al. Among authors: tantravahi u. Neurology. 1990 Aug;40(8):1267-70. doi: 10.1212/wnl.40.8.1267. Neurology. 1990. PMID: 2199849

4

Characterization of microsatellite polymorphisms DXS691 and DXS692: genetic mapping to Xq26.2-Xq27 and Xq25-Xq26.2.

Lasser DM, Wilhelmsen KC, Nygaard TG, Tantravahi U. Lasser DM, et al. Among authors: tantravahi u. Genomics. 1993 Jun;16(3):785-6. doi: 10.1006/geno.1993.1269. Genomics. 1993. PMID: 8325656 Free article. No abstract available.

5

A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis.

Burmeister M, Kim S, Price ER, de Lange T, Tantravahi U, Myers RM, Cox DR. Burmeister M, et al. Among authors: tantravahi u. Genomics. 1991 Jan;9(1):19-30. doi: 10.1016/0888-7543(91)90216-2. Genomics. 1991. PMID: 2004760

6

Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes.

Tantravahi U, Stewart GD, Van Keuren M, McNeil G, Roy S, Patterson D, Drabkin H, Lalande M, Kurnit DM, Latt SA. Tantravahi U, et al. Hum Genet. 1988 Jul;79(3):196-202. doi: 10.1007/BF00366237. Hum Genet. 1988. PMID: 3402991 Free article.

7

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.

Tantravahi U, Nicholls RD, Stroh H, Ringer S, Neve RL, Kaplan L, Wharton R, Wurster-Hill D, Graham JM Jr, Cantú ES, et al. Tantravahi U, et al. Am J Med Genet. 1989 May;33(1):78-87. doi: 10.1002/ajmg.1320330110. Am J Med Genet. 1989. PMID: 2750788

8

Radiation hybrids for the proximal long arm of the X chromosome and their use in the derivation of an ordered set of cosmid markers from a defined subregion in proximal Xq13.1.

Röhme D, Sidén T, van der Maarel SM, Cremers FP, Tantravahi U, Marinoni JC, Ropers HH, Schwartz CE. Röhme D, et al. Among authors: tantravahi u. Somat Cell Mol Genet. 1994 Jan;20(1):1-10. doi: 10.1007/BF02257481. Somat Cell Mol Genet. 1994. PMID: 8197472

9

Parental imprinting of an Igf-2 transgene.

Lee JE, Tantravahi U, Boyle AL, Efstratiadis A. Lee JE, et al. Among authors: tantravahi u. Mol Reprod Dev. 1993 Aug;35(4):382-90. doi: 10.1002/mrd.1080350411. Mol Reprod Dev. 1993. PMID: 8398116

10

Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22.

Arheden K, Tantravahi U, Tommerup N, Tranebjaerg L, Mitelman F. Arheden K, et al. Among authors: tantravahi u. Hereditas. 1989;110(3):253-65. doi: 10.1111/j.1601-5223.1989.tb00787.x. Hereditas. 1989. PMID: 2753742 Free article.

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