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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

430 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
No association between the APOE gene and autism.
Raiford KL, Shao Y, Allen IC, Martin ER, Menold MM, Wright HH, Abramson RK, Worley G, DeLong GR, Vance JM, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Raiford KL, et al. Among authors: gilbert jr. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):57-60. doi: 10.1002/ajmg.b.20104. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755445
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.
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.
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
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.
430 results