Gilbert JR - Search Results

1

Linkage studies of late-onset familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Among authors: gilbert jr. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 No abstract available.

2

Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis.

Samson F, de Jong PJ, Trask BJ, Koza-Taylor P, Speer MC, Potter T, Roses AD, Gilbert JR. Samson F, et al. Among authors: gilbert jr. Genomics. 1992 Aug;13(4):1374-5. doi: 10.1016/0888-7543(92)90077-6. Genomics. 1992. PMID: 1505979 No abstract available.

3

The identification and characterization of KRAB-domain-containing zinc finger proteins.

Constantinou-Deltas CD, Gilbert J, Bartlett RJ, Herbstreith M, Roses AD, Lee JE. Constantinou-Deltas CD, et al. Genomics. 1992 Mar;12(3):581-9. doi: 10.1016/0888-7543(92)90451-w. Genomics. 1992. PMID: 1559709

4

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

Sarfarazi M, Wijmenga C, Upadhyaya M, Weiffenbach B, Hyser C, Mathews K, Murray J, Gilbert J, Pericak-Vance M, Lunt P, et al. Sarfarazi M, et al. Am J Hum Genet. 1992 Aug;51(2):396-403. Am J Hum Genet. 1992. PMID: 1642237 Free PMC article.

5

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al. Gilbert JR, et al. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.

6

A PstI polymorphism detected by a genomic clone at the human slow troponin T (TNNT1) gene locus.

Samson F, Gilbert JR, Koza-Taylor P, Speer MC, Lee J, Roses AD. Samson F, et al. Among authors: gilbert jr. Nucleic Acids Res. 1991 Nov 11;19(21):6058. doi: 10.1093/nar/19.21.6058. Nucleic Acids Res. 1991. PMID: 1682896 Free PMC article.

7

Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA.

Samson F, Lee JE, Hung WY, Potter TG, Herbstreith M, Roses AD, Gilbert JR. Samson F, et al. Among authors: gilbert jr. J Neurosci Res. 1990 Dec;27(4):441-51. doi: 10.1002/jnr.490270403. J Neurosci Res. 1990. PMID: 1706783

8

Inherited deletion at Duchenne dystrophy locus in normal male.

Koh J, Bartlett RJ, Pericak-Vance MA, Speer MC, Yamaoka LH, Phillips K, Hung WY, Ray PN, Worton RG, Gilbert JR, et al. Koh J, et al. Among authors: gilbert jr. Lancet. 1987 Nov 14;2(8568):1154-5. doi: 10.1016/s0140-6736(87)91590-x. Lancet. 1987. PMID: 2890056 No abstract available.

9

A Bgl II polymorphism detected by LDR152 [D19S19].

Walker AP, Bartlett RJ, Yamaoka LH, Secore SL, Lee JE, Gilbert J, Herbstreith M, Pericak-Vance MA, Hung WY, Roses AD. Walker AP, et al. Nucleic Acids Res. 1988 Sep 26;16(18):9063. doi: 10.1093/nar/16.18.9063. Nucleic Acids Res. 1988. PMID: 2902564 Free PMC article.

10

A new probe for the diagnosis of myotonic muscular dystrophy.

Bartlett RJ, Pericak-Vance MA, Yamaoka L, Gilbert J, Herbstreith M, Hung WY, Lee JE, Mohandas T, Bruns G, Laberge C, et al. Bartlett RJ, et al. Science. 1987 Mar 27;235(4796):1648-50. doi: 10.1126/science.3029876. Science. 1987. PMID: 3029876

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