Dietz-Band J - Search Results

1

Dinucleotide repeat polymorphism at the human chromosome 11p telomere (D11S2071).

Browne DL, Smith EA, Dietz-Band J, Riethmann HC, Phromchotikul T, Litt M. Browne DL, et al. Among authors: dietz band j. Genomics. 1995 Jan 20;25(2):600-1. doi: 10.1016/0888-7543(95)80071-s. Genomics. 1995. PMID: 7790003 No abstract available.

2

A 500-kb physical map and contig from the Harvey ras-1 gene to the 11p telomere.

Russell MW, Munroe DJ, Bric E, Housman DE, Dietz-Band J, Riethman HC, Collins FS, Brody LC. Russell MW, et al. Among authors: dietz band j. Genomics. 1996 Jul 15;35(2):353-60. doi: 10.1006/geno.1996.0367. Genomics. 1996. PMID: 8661149

3

Characterization of polymorphic loci on a telomeric fragment of DNA from the long arm of human chromosome 7.

Dietz-Band J, Riethman H, Hildebrand CE, Moyzis R. Dietz-Band J, et al. Genomics. 1990 Sep;8(1):168-70. doi: 10.1016/0888-7543(90)90240-u. Genomics. 1990. PMID: 2081591

4

Isolation, characterization, and physical localization of 33 human X-chromosome RFLP markers.

Dietz-Band JN, Turco AE, Willard HF, Vincent A, Skolnick MH, Barker DF. Dietz-Band JN, et al. Cytogenet Cell Genet. 1990;54(3-4):137-41. doi: 10.1159/000132977. Cytogenet Cell Genet. 1990. PMID: 1979940

5

High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers.

Barker DF, Fain PR, Goldgar DE, Dietz-Band JN, Turco AE, Kashtan CE, Gregory MC, Tryggvason K, Skolnick MH, Atkin CL. Barker DF, et al. Among authors: dietz band jn. Hum Genet. 1991 Dec;88(2):189-94. doi: 10.1007/BF00206070. Hum Genet. 1991. PMID: 1684566

6

Molecular genetic analysis of the 3p- syndrome.

Phipps ME, Latif F, Prowse A, Payne SJ, Dietz-Band J, Leversha M, Affara NA, Moore AT, Tolmie J, Schinzel A, et al. Phipps ME, et al. Among authors: dietz band j. Hum Mol Genet. 1994 Jun;3(6):903-8. doi: 10.1093/hmg/3.6.903. Hum Mol Genet. 1994. PMID: 7951234 Free article. Clinical Trial.

7

Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome.

Muenke M, Bone LJ, Mitchell HF, Hart I, Walton K, Hall-Johnson K, Ippel EF, Dietz-Band J, Kvaløy K, Fan CM, et al. Muenke M, et al. Among authors: dietz band j. Am J Hum Genet. 1995 Nov;57(5):1074-9. Am J Hum Genet. 1995. PMID: 7485157 Free PMC article.

8

Norman-Roberts syndrome: clinical and molecular studies.

Iannetti P, Schwartz CE, Dietz-Band J, Light E, Timmerman J, Chessa L. Iannetti P, et al. Among authors: dietz band j. Am J Med Genet. 1993 Aug 1;47(1):95-9. doi: 10.1002/ajmg.1320470120. Am J Med Genet. 1993. PMID: 8368261 Review.

9

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

Gurrieri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Schindler D, Dietz-Band J, Vergnaud G, Scherer SW, et al. Gurrieri F, et al. Among authors: dietz band j. Nat Genet. 1993 Mar;3(3):247-51. doi: 10.1038/ng0393-247. Nat Genet. 1993. PMID: 8485580

10

Amplification and overexpression of HER-2/neu in carcinomas of the salivary gland: correlation with poor prognosis.

Press MF, Pike MC, Hung G, Zhou JY, Ma Y, George J, Dietz-Band J, James W, Slamon DJ, Batsakis JG, et al. Press MF, et al. Among authors: dietz band j. Cancer Res. 1994 Nov 1;54(21):5675-82. Cancer Res. 1994. PMID: 7522962

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