Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

427 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 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.
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.
Myotonic dystrophy: update on progress to define the gene.
Roses AD, Pericak-Vance MA, Bartlett RJ, Yamaoka LH, Lee JE, Koh J, Chen JC, Gilbert JR, Ross DA, Herbstreith MH, et al. Roses AD, et al. Among authors: gilbert jr. Aust Paediatr J. 1988;24 Suppl 1:66-9. Aust Paediatr J. 1988. PMID: 3060077 Review.
A de novo frame-shift mutation in the tuberin gene.
Kumar A, Wolpert C, Kandt RS, Segal J, Pufky J, Roses AD, Pericak-Vance MA, Gilbert JR. Kumar A, et al. Among authors: gilbert jr. Hum Mol Genet. 1995 Aug;4(8):1471-2. doi: 10.1093/hmg/4.8.1471. Hum Mol Genet. 1995. PMID: 7581393 No abstract available.
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.
Speer MC, Tandan R, Rao PN, Fries T, Stajich JM, Bolhuis PA, Jöbsis GJ, Vance JM, Viles KD, Sheffield K, James C, Kahler SG, Pettenati M, Gilbert JR, Denton PH, Yamaoka LH, Pericak-Vance MA. Speer MC, et al. Among authors: gilbert jr. Hum Mol Genet. 1996 Jul;5(7):1043-6. doi: 10.1093/hmg/5.7.1043. Hum Mol Genet. 1996. PMID: 8817344
A novel splice site mutation (156 + 1G-->A) in the TSC2 gene.
Kumar A, Kandt RS, Wolpert C, Roses AD, Pericak-Vance MA, Gilbert JR. Kumar A, et al. Among authors: gilbert jr. Hum Mutat. 1997;9(1):64-5. doi: 10.1002/(SICI)1098-1004(1997)9:1<64::AID-HUMU12>3.0.CO;2-N. Hum Mutat. 1997. PMID: 8990012 No abstract available.
427 results