Hejtmancik JF - Search Results

1

Exclusion of Usher syndrome gene from much of chromosome 4.

Smith RJ, Holcomb JD, Daiger SP, Caskey CT, Pelias MZ, Alford BR, Fontenot DD, Hejtmancik JF. Smith RJ, et al. Among authors: hejtmancik jf. Cytogenet Cell Genet. 1989;50(2-3):102-6. doi: 10.1159/000132733. Cytogenet Cell Genet. 1989. PMID: 2776474

2

Clinical variability and genetic heterogeneity within the Acadian Usher population.

Smith RJ, Pelias MZ, Daiger SP, Keats B, Kimberling W, Hejtmancik JF. Smith RJ, et al. Among authors: hejtmancik jf. Am J Med Genet. 1992 Aug 1;43(6):964-9. doi: 10.1002/ajmg.1320430612. Am J Med Genet. 1992. PMID: 1415347

3

Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26).

Huang TH, Hejtmancik JF, Edwards A, Pettigrew AL, Herrera CA, Hammond HA, Caskey CT, Zoghbi HY, Ledbetter DH. Huang TH, et al. Among authors: hejtmancik jf. Am J Hum Genet. 1991 Dec;49(6):1312-9. Am J Hum Genet. 1991. PMID: 1746558 Free PMC article.

4

Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.

Ward PA, Hejtmancik JF, Witkowski JA, Baumbach LL, Gunnell S, Speer J, Hawley P, Tantravahi U, Caskey CT. Ward PA, et al. Among authors: hejtmancik jf. Am J Hum Genet. 1989 Feb;44(2):270-81. Am J Hum Genet. 1989. PMID: 2643315 Free PMC article.

5

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.

Wayne S, Der Kaloustian VM, Schloss M, Polomeno R, Scott DA, Hejtmancik JF, Sheffield VC, Smith RJ. Wayne S, et al. Among authors: hejtmancik jf. Hum Mol Genet. 1996 Oct;5(10):1689-92. doi: 10.1093/hmg/5.10.1689. Hum Mol Genet. 1996. PMID: 8894709

6

Fine mapping of the usher syndrome type IC to chromosome 11p14 and identification of flanking markers by haplotype analysis.

Ayyagari R, Li Y, Smith RJ, Pelias MZ, Hejtmancik JF. Ayyagari R, et al. Among authors: hejtmancik jf. Mol Vis. 1995 Oct 25;1:2. Mol Vis. 1995. PMID: 9238080 Free article.

7

Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium.

Keats BJ, Todorov AA, Atwood LD, Pelias MZ, Hejtmancik JF, Kimberling WJ, Leppert M, Lewis RA, Smith RJ. Keats BJ, et al. Among authors: hejtmancik jf. Genomics. 1992 Nov;14(3):707-14. doi: 10.1016/s0888-7543(05)80172-7. Genomics. 1992. PMID: 1427898

8

In vitro amplification of the alpha 1-antitrypsin gene: application to prenatal diagnosis.

Hejtmancik JF, Holcomb JD, Howard J, Vanderford M. Hejtmancik JF, et al. Prenat Diagn. 1989 Mar;9(3):177-86. doi: 10.1002/pd.1970090306. Prenat Diagn. 1989. PMID: 2785265

9

Diagnosis of human heritable defects by recombinant DNA methods.

Caskey CT, Gibbs RA, Witkowski JA, Hejtmancik JF. Caskey CT, et al. Among authors: hejtmancik jf. Philos Trans R Soc Lond B Biol Sci. 1988 Jun 15;319(1194):353-60. doi: 10.1098/rstb.1988.0056. Philos Trans R Soc Lond B Biol Sci. 1988. PMID: 2900528 Review.

10

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium.

Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA, Möller CG, Pelias MZ, Tranebjaerg L. Smith RJ, et al. Among authors: hejtmancik jf. Am J Med Genet. 1994 Mar 1;50(1):32-8. doi: 10.1002/ajmg.1320500107. Am J Med Genet. 1994. PMID: 8160750

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