Hejtmancik JF - Search Results

1

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M. Towbin JA, et al. Among authors: hejtmancik jf. Circulation. 1993 Jun;87(6):1854-65. doi: 10.1161/01.cir.87.6.1854. Circulation. 1993. PMID: 8504498

2

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population.

Hejtmancik JF, Brink PA, Towbin J, Hill R, Brink L, Tapscott T, Trakhtenbroit A, Roberts R. Hejtmancik JF, et al. Circulation. 1991 May;83(5):1592-7. doi: 10.1161/01.cir.83.5.1592. Circulation. 1991. PMID: 2022018

3

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Towbin JA, Li H, Taggart RT, Lehmann MH, Schwartz PJ, Satler CA, Ayyagari R, Robinson JL, Moss A, Hejtmancik JF. Towbin JA, et al. Among authors: hejtmancik jf. Circulation. 1994 Dec;90(6):2635-44. doi: 10.1161/01.cir.90.6.2635. Circulation. 1994. PMID: 7994803

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

Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening.

Jinks DC, Minter M, Tarver DA, Vanderford M, Hejtmancik JF, McCabe ER. Jinks DC, et al. Among authors: hejtmancik jf. Hum Genet. 1989 Mar;81(4):363-6. doi: 10.1007/BF00283692. Hum Genet. 1989. PMID: 2703239

6

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.

7

X-linked infantile spinal muscular atrophy.

Greenberg F, Fenolio KR, Hejtmancik JF, Armstrong D, Willis JK, Shapira E, Huntington HW, Haun RL. Greenberg F, et al. Among authors: hejtmancik jf. Am J Dis Child. 1988 Feb;142(2):217-9. doi: 10.1001/archpedi.1988.02150020119045. Am J Dis Child. 1988. PMID: 3341327

8

Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.

Parolini O, Hejtmancik JF, Allen RC, Belmont JW, Lassiter GL, Henry MJ, Barker DF, Conley ME. Parolini O, et al. Among authors: hejtmancik jf. Genomics. 1993 Feb;15(2):342-9. doi: 10.1006/geno.1993.1066. Genomics. 1993. PMID: 8449500

9

A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus.

Chen JD, Hejtmancik JF, Romeo G, Lindlof M, Boehm C, Caskey CT, Kress W, Fischbeck KH, Dreier M, Serravalle S, et al. Chen JD, et al. Among authors: hejtmancik jf. Genomics. 1989 Jan;4(1):105-9. doi: 10.1016/0888-7543(89)90322-4. Genomics. 1989. PMID: 2563349

10

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

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